Clearance Summary
CATAPRESS TOURNIGUET received FDA 510(k) clearance under submission number K852277, sponsored by Boehringer Ingelheim Pharmaceuticals, 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 1985-06-27.
- Submission: K852277
- Applicant / Sponsor: Boehringer Ingelheim Pharmaceuticals, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.5900
- Decision date: 1985-06-27
Classification & Regulation
This clearance is catalogued under FDA product code GAX and 21 CFR 878.5900, within the General, Plastic Surgery review panel as a Class I device.