21 C.F.R. § 886.3920

Current through September 30, 2024
Section 886.3920 - Aqueous shunt
(a)Identification. An aqueous shunt is an implantable device intended to reduce intraocular pressure in the anterior chamber of the eye in patients with neovascular glaucoma or with glaucoma when medical and conventional surgical treatments have failed.
(b)Classification. Class II. The special controls for this device are FDA's:
(1) "Use of International Standard ISO 10993 'Biological Evaluation of Medical Devices-Part I: Evaluation and Testing,' "
(2) "510(k) Sterility Review Guidance of 2/12/90 (K90-1)," and
(3) "Aqueous Shunts-510(k) Submissions."

21 C.F.R. §886.3920

65 FR 17147, Mar. 31, 2000, as amended at 66 FR 18542, Apr. 10, 2001