Clearance Summary
NEW TRAVENOL ROLLER CLAMP-SOLUTION ADMIN. SET received FDA 510(k) clearance under submission number K854517, sponsored by Travenol Laboratories, S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1985-12-02.
- Submission: K854517
- Applicant / Sponsor: Travenol Laboratories, S.A.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.4730
- Decision date: 1985-12-02
Classification & Regulation
This clearance is catalogued under FDA product code FKK and 21 CFR 876.4730, within the Gastroenterology, Urology review panel as a Class I device.