Clearance Summary
3.0T 16ch AIR AA received FDA 510(k) clearance under submission number K223378, sponsored by Ge Healthcare Coils (Usa Instruments, Inc.). The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-01-03.
- Submission: K223378
- Applicant / Sponsor: Ge Healthcare Coils (Usa Instruments, Inc.)
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 2023-01-03
Classification & Regulation
This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.