Clearance Summary
BRIOX MODEL 2000-CA COMPRESSOR UNIT received FDA 510(k) clearance under submission number K791241, sponsored by Briox Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1979-07-24.
- Submission: K791241
- Applicant / Sponsor: Briox Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4780
- Decision date: 1979-07-24
Classification & Regulation
This clearance is catalogued under FDA product code JCX and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.