Clearance Summary
MOBILE C-ARM OMNI 325 received FDA 510(k) clearance under submission number K880518, sponsored by Fischer Imaging Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1988-03-09.
- Submission: K880518
- Applicant / Sponsor: Fischer Imaging Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 1988-03-09
Classification & Regulation
This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.