Clearance Summary
PERIDIAL PERITONEAL DIALYSIS TRAY received FDA 510(k) clearance under submission number K792207, sponsored by Cutter 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 1979-12-10.
- Submission: K792207
- Applicant / Sponsor: Cutter Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5820
- Decision date: 1979-12-10
Classification & Regulation
This clearance is catalogued under FDA product code FKG and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class I device.