Clearance Summary
NEO-CARE PERITONEAL DIALYSIS ADMINISTRATION SET received FDA 510(k) clearance under submission number K972731, sponsored by Klein-Baker Medical, 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 1997-09-29.
- Submission: K972731
- Applicant / Sponsor: Klein-Baker Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5630
- Decision date: 1997-09-29
Classification & Regulation
This clearance is catalogued under FDA product code KDJ and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.