Clearance Summary
CHROMOPHARE D 500, CHROMOPHARE D 530 received FDA 510(k) clearance under submission number K974433, sponsored by Berchtold Holding GmbH. 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 1998-02-20.
- Submission: K974433
- Applicant / Sponsor: Berchtold Holding GmbH
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4580
- Decision date: 1998-02-20
Classification & Regulation
This clearance is catalogued under FDA product code FSY and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.