Clearance Summary
MINI 6800 DIGITAL MOBILE C-ARM received FDA 510(k) clearance under submission number K992506, sponsored by Ge Dec Medical Systems. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1999-08-19.
- Submission: K992506
- Applicant / Sponsor: Ge Dec Medical Systems
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 1999-08-19
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.