Clearance Summary
OSTOMY OR UROSTOMY ABDOMINAL BELT OS received FDA 510(k) clearance under submission number K842119, sponsored by Atlas Surgical Belt Co., 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 1984-09-10.
- Submission: K842119
- Applicant / Sponsor: Atlas Surgical Belt Co., Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5900
- Decision date: 1984-09-10
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.