Ex Parte BrownDownload PDFPatent Trial and Appeal BoardAug 25, 201711226404 (P.T.A.B. Aug. 25, 2017) Copy Citation United States Patent and Trademark Office UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O.Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 7553.00115/05-0900 4380 EXAMINER JIAN, SHIRLEY XUEYING ART UNIT PAPER NUMBER 3769 MAIL DATE DELIVERY MODE 11/226,404 09/15/2005 60683 7590 Robert Bosch LLC 1800 W. Central Road Mount Prospect, IL 60056 Stephen J. Brown 08/28/2017 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte STEPHEN J. BROWN Appeal 2016-001013 Application 11/226,404 Technology Center 3700 Before HUBERT C. LORIN, BIBHU R. MOHANTY, and BRUCE T. WIEDER, Administrative Patent Judges. LORIN, Administrative Patent Judge. DECISION ON APPEAL STATEMENT OF THE CASE Appellant1 appeals under 35 U.S.C. § 134(a) from the Examiner’s rejection of claims 54—61, 63—66, and 68—77. We have jurisdiction under 35 U.S.C. § 6(b). SUMMARY OF DECISION We AFFIRM-IN-PART. 1 Appellant identifies Robert Bosch Healthcare Systems, Inc. as the real party in interest (Appeal Br. 2). Appeal 2016-001013 Application 11/226,404 THE INVENTION Appellant’s claimed invention relates to a remote health monitoring and maintenance system that enables a bi-directional interaction between a patient and a health care provider (Spec. 1: 14—16). Claim 54, reproduced below with bracketed numerals added, is illustrative of the subject matter on appeal. 54. A healthcare data monitoring and management system, comprising: [1] one or more physiological monitoring devices, each producing healthcare data representative of the health of a person; [2] a handheld unit configured to receive said healthcare data from at least one of the physiological monitoring devices in response to executing a computer-executable program and transmit the healthcare data over a communication network in response to executing the computer-executable program, said handheld unit comprising a display allowing the person to view the healthcare data and a speaker allowing the person to hear the healthcare data; [3] a clearinghouse configured to receive the healthcare data from the handheld unit and format the healthcare data to be reviewed remotely through an interactive website over the communication network by a healthcare provider using a computer; and [4] a database in communication with said clearinghouse and configured to (i) store the healthcare data received by the clearinghouse from the handheld unit and (ii) provide said healthcare data to the healthcare provider via the clearinghouse. THE REJECTION The Examiner relies on the following as evidence of unpatentability: Bomn et al. US 5,348,008 Sept. 20, 1994 2 Appeal 2016-001013 Application 11/226,404 (“Bomn”) Ballantyne et al. US 5,867,821 Feb. 2, 1999 (“Ballantyne”) Moshfeghi et al. US 6,076,166 June 13,2000 (“Moshfeghi”) Claims 54—61, 63—66, and 68—77 are rejected under 35 U.S.C. § 103 as being unpatentable over Bomn, Ballantyne, and Moshfeghi. ANALYSIS Priority Appellant argues that Ballantyne and Moshfeghi are not available as prior art because this application is entitled to a priority date of November 17, 1992, which antedates Ballantyne and Moshfeghi (Appeal Br. 7, 9—10; Reply Br. 2—3). Appellant has made a claim of priority to Application No. 07/977,323 (now US Patent No. 5,307,263) under 35 U.S.C. § 120 {see Spec. 1, lines 3—12). In order for the claims on appeal to be entitled to the benefit of the filing dates of the ’323 application under 35 U.S.C. §120, the record must show that the ’323 application contains a disclosure which complies with 35 U.S.C. § 112, first paragraph, for each claim in the subsequently filed ’404 application. Studiengesellschaft Kohle, M.B.H. v. Shell Oil Co., 112 F.3d 1561, 1564—65 (Fed. Cir. 1997). According to Appellant, “[a]s exemplified by FIG. 1, column 7 line 29 through column 12 line 28 of the ’263 patent, each limitation of claim 1 [sic — claim 54] is disclosed in the ’263 patent.” (Appeal Br. 7, 9). In contrast, the Examiner finds that “for claim features [3] and [4], support is not found in any other parent applications/patents; except, US Patent No. 7,624,028 which has a priority date of 03/17/1999.” (Ans. 11— 3 Appeal 2016-001013 Application 11/226,404 12). The Examiner therefore determines that the claims are entitled to an earliest priority date of March 17, 1999 and that Ballantyne and Moshfeghi are available as prior art. We agree with the Examiner. Independent claims 54, 63, and 70 each requires formatting data to be reviewed “through an interactive website.” Appellant has not pointed to any support in the ’263 patent for this limitation (Appeal Br. 7, 9-10; Reply Br. 2—3). We have reviewed the ’263 patent and find that it does not provide support for formatting data to be reviewed “through an interactive website.” The ’263 patent does not contain any disclosure of any website, web server, or web browser, much less an interactive website. Accordingly, we sustain the Examiner’s finding that the claims of this application are not entitled to the priority date of the ’323 application (’263 patent). Consequently, we also find that the Appellant has not persuasively shown that Ballantyne and Moshfeghi are not available as prior art. Obviousness Independent claim 54 Appellant argues that “Ballantyne does not disclose the transfer of ‘healthcare data’ as that term is used in the claim” because Ballantyne’s data is not “produced by a physiological machine as required by claim 54” (Appeal Br. 7). Appellant also contends that “the PDA of Ballantyne is not a physiological monitoring device” (Reply Br. 5). The Examiner finds the “physiological monitoring devices, each producing healthcare data” limitation of claim 54 in Bomn (Ans. 3). 4 Appeal 2016-001013 Application 11/226,404 Appellant’s arguments that Ballantyne does not disclose “healthcare data” and “a physiological monitoring device” do not address the Examiner’s findings in Bomn. The Examiner only relied on Ballantyne’s PDA units to show the claimed data path to the clearinghouse “from the handheld unit” (i.e., instead of Bomn’s direct path from patient unit 1000 to central base station 2000) (Ans. 4—5; 12—13). The Appellant contends that “the Examiner has failed to provide a clear articulation explaining why it would be obvious” to modify Bomn “to transmit healthcare data from a portable device” (Appeal Br. 9). The Appellant argues that, because of the direct path from the patient unit 1000 to the central base station 2000 in Bomn, “any healthcare data in the nurse’s unit is already present in the central base station 2000 prior to any communication from the nurse unit 3000” (Appeal Br. 8). According to the Appellant, “[sjince the most recent healthcare data is at the central base, there is no purpose behind retransmitting the data to the central base after the central base transmits the data to the nurse unit” (Appeal Br. 8—9). Appellant also contends that “[t]he nurse’s unit is not a physiological monitoring device” and “[tjherefore, the nurse’s annotations are not healthcare data as required by claim 54.” {Id. at 9). According to Appellant, “[sjimply making notes in a device does not transform that device into a ‘physiological monitoring device.’” (Reply Br. 5). The Examiner finds the claimed “physiological monitoring device” in patient units 1000 of Bomn (Ans. 3), not in Bomn’s nurse units 3000 or Ballantyne’s PDA 420. Thus, Appellant’s arguments that the nurse units are not physiological monitoring devices do not address the Examiner’s finding. 5 Appeal 2016-001013 Application 11/226,404 The Examiner’s discussion of using the PDA disclosed in Ballantyne is to provide a motivation for modifying the data path of Bomn to include a handheld device. According to the Examiner, “it is necessary to transmit patient’s healthcare data from the nurse unit to the central monitoring station to ensure the latest record of patient data is kept since nurses often modify/mark specific events to a patient’s healthcare data.” (Ans. 5). Ballantyne discloses that medical personnel can update medical records using a handheld PDA tablet display 420. For example, Ballantyne discloses that “new information is entered through the PDA technology by simply writing as normal on the pen display tablet” (Ballantyne col. 14, lines 19— 26). Ballantyne further discloses that this additional or modified data must be transferred to the nursing station 418 (see, e.g., Ballantyne col. 12, lines 48—63). Appellant’s argument that “the nurse’s annotations are not healthcare data” is not persuasive because nothing in claim 54 excludes a nurse’s annotations from being added to existing healthcare data (i.e., data produced by patient units 1000) that is transferred to a handheld unit. Appellant’s argument that there is “no purpose” for the combination is not persuasive because it ignores the Examiner’s articulated reasoning. Accordingly, we find that the Examiner clearly articulated a reason for the proposed combination of Bomn and Ballantyne. The Appellant further argues that “the Examiner has failed to provide a clear articulation” for the combination of Bomn and Moshfeghi (Appeal Br. 10-11). According to the Appellant, “[ajdding verification protocols, and limiting the individuals who can receive the data which has been determined to be indicative of a life-threatening situation, would 6 Appeal 2016-001013 Application 11/226,404 unacceptably delay the receipt of alerts in the system of Bomn” (Id. at 10). Appellant contends that “while the protocols and security layers provided by Moshfeghi are suitable for stored confidential material as intended by the system of Moshfeghi (see, e.g., Moshfeghi at Abstract), such protocols are not suitable for an alert system dealing with real-time life-threatening situations” (Id.). Appellant’s argument is not persuasive because it amounts to attorney argument, not record evidence sufficient to rebut the Examiner’s prima facie case of obviousness. See In re Geisler, 116 F.3d 1465, 1470 (Fed. Cir. 1997) (Attorney argument cannot take the place of record evidence.). For the foregoing reasons, the Appellant’s arguments as to error in the rejection is unpersuasive. Accordingly, the rejection of claim 54 under 35 U.S.C. § 103(a) as being unpatentable over Bomn, Ballantyne, and Moshfeghi is sustained. Because the arguments with respect to independent claims 63 and 70 and dependent claims 56—58, 60, 61, 65, 66, 68, 69, and 72—77 (Appeal Br. 6—18; Reply Br. 2—6) are the same, we sustain the rejection of those claims for the same reasons. Dependent claims 55, 64, and 71 Claim 55 depends from claim 54 and recites “wherein said clearinghouse comprises a computer server.” The Appellant contends that the rejection of claim 55 is improper “because not all computers are servers, Bomn’s computer is not necessarily a server.” According to the Appellant, “[i]t is well-known, however, that 7 Appeal 2016-001013 Application 11/226,404 ‘servers’ are specialized computers which ‘operate within a client-server architecture.’” (Appeal Br. 12). The Examiner finds that “Bomn teaches a client-server architecture in Fig. 1 A. Specifically, the central base station 2000 is a server computer that is in two way communication with a plurality of client devices including patient devices 1000 and nurse units 3000.” (Ans. 17). The Appellant has not addressed this finding by the Examiner and the Appellant’s argument therefore does not apprise us of error in the Examiner’s rejection of claim 55. Accordingly, we sustain the rejection of dependent claim 55. Because the Appellant’s arguments with respect to dependent claims 64 and 71 are the same (Appeal Br. 16,18), we sustain the rejection of those claims for the same reasons. Dependent claim 59 Claim 59 depends from claim 54 and recites “wherein the handheld unit is a compact, portable unit adapted to patient self-care.” The Examiner finds that “Bomn teaches a remote dispatcher station that is handheld, compact and portable” (Ans. 18). The Appellant argues, inter alia, that “Bomn [] teaches that a remote dispatcher station includes a personal computer, a full screen display, a printer, and other components. A personal computer with a full screen display and printer is neither handheld nor portable.” (Reply Br. 6) (citing Bomn col. 15, lines 28—29). Dispatcher station 5000, as shown in Figure 2 A of Bomn, includes display 5004, which is described as a “full screen PC display 5004” (Bomn 8 Appeal 2016-001013 Application 11/226,404 col. 15, lines 28—29), i.e., a personal computer (“PC”) display. Therefore, we agree with the Appellant that dispatcher station 5000 is not a “handheld unit [that] is a compact, portable unit” as required by claim 59. Accordingly, we do not sustain the rejection of claim 59. DECISION The rejection of claims 54—58, 60, 61, 63—66, and 68—77 under 35 U.S.C. § 103 is affirmed. The rejection of claim 59 under 35 U.S.C. § 103 is reversed. No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a). AFFIRMED-IN-PART 9 Copy with citationCopy as parenthetical citation