Clearance Summary
MOBILE C-ARM received FDA 510(k) clearance under submission number K121303, sponsored by Canon Inc. -Medical Equipment Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-07-26.
- Submission: K121303
- Applicant / Sponsor: Canon Inc. -Medical Equipment Group
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 2012-07-26
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.