Clearance Summary
BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE received FDA 510(k) clearance under submission number K963950, sponsored by Bioderm, Inc.. 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 1997-01-10.
- Submission: K963950
- Applicant / Sponsor: Bioderm, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5250
- Decision date: 1997-01-10
Classification & Regulation
This clearance is catalogued under FDA product code EXI and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class I device.