FDA 510(k), K923065, BAXTER PERSONAL CYCLER AUTOMMATED PERITONEAL DIAL

510(K) Number: K923065
Device Name: BAXTER PERSONAL CYCLER AUTOMMATED PERITONEAL DIAL
Manufacturer: BAXTER HEALTHCARE CORP.
Device Classification Name: system, peritoneal, automatic delivery
Regulation Number: 876.5630
Classification Product Code: FKX
Date Received: 06/25/1992
Decision Date: 03/04/1994
Regulation Medical Specialty: Gastroenterology/Urology

Total pages: 735
Fully redacted pages: 612
Content pages: 123