21 C.F.R. § 892.1000

Magnetic resonance diagnostic device.

Last amended: 2019Year: 2026Length: 131 wordsSubsections: 2Official source

Cite as 21 C.F.R. § 892.1000 (2026)

(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. [53 FR 5078, Feb. 1, 1989, as amended at 84 FR 71818, Dec. 30, 2019]
Cross-references to the CFR
892.9.
21 C.F.R. § 892.1000: Magnetic resonance diagnostic device. | Justis AI