Clearance Summary
AMP CAPD UNISPIKE AMINISTRATION SET received FDA 510(k) clearance under submission number K822551, sponsored by American Medical Products, 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 1982-10-13.
- Submission: K822551
- Applicant / Sponsor: American Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.4730
- Decision date: 1982-10-13
Classification & Regulation
This clearance is catalogued under FDA product code FKK and 21 CFR 876.4730, within the Gastroenterology, Urology review panel as a Class I device.