Clearance Summary
ODOR-SAFE(TM)(LIQUID) ODOR-SAFE(TM) POWDER received FDA 510(k) clearance under submission number K871526, sponsored by Cox Family Laboratories, 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 1987-10-13.
- Submission: K871526
- Applicant / Sponsor: Cox Family Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5900
- Decision date: 1987-10-13
Classification & Regulation
This clearance is catalogued under FDA product code EXB and 21 CFR 876.5900, within the Gastroenterology, Urology review panel as a Class I device.