Clearance Summary
CONVATEC ABSORBENT BANDAGE received FDA 510(k) clearance under submission number K904233, sponsored by Convatec, A Division of E.R. Squibb & Sons. 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 1991-03-06.
- Submission: K904233
- Applicant / Sponsor: Convatec, A Division of E.R. Squibb & Sons
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5900
- Decision date: 1991-03-06
Classification & Regulation
This clearance is catalogued under FDA product code EXE and 21 CFR 876.5900, within the Gastroenterology, Urology review panel as a Class I device.