Clearance Summary
MOBIL C-ARM, REGURBISHED, VARIOUS MODELS received FDA 510(k) clearance under submission number K950971, sponsored by Pro-Tronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1995-04-11.
- Submission: K950971
- Applicant / Sponsor: Pro-Tronics, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 1995-04-11
Classification & Regulation
This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.