21 C.F.R. § 892.1000

Current through October 31, 2024
Section 892.1000 - Magnetic resonance diagnostic device
(a)Identification. A magnetic resonance diagnostic device is intended for general diagnostic use to present images which reflect the spatial distribution and/or magnetic resonance spectra which reflect frequency and distribution of nuclei exhibiting nuclear magnetic resonance. Other physical parameters derived from the images and/or spectra may also be produced. The device includes hydrogen-1 (proton) imaging, sodium-23 imaging, hydrogen-1 spectroscopy, phosphorus-31 spectroscopy, and chemical shift imaging (preserving simultaneous frequency and spatial information).
(b)Classification. Class II (special controls). A magnetic resonance imaging disposable kit intended for use with a magnetic resonance diagnostic device only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9 .

21 C.F.R. §892.1000

53 FR 5078, Feb. 1, 1989, as amended at 84 FR 71818 , Dec. 30, 2019
As amended at 84 FR 71818, 12/30/2019