FDA 510(k), K902149, FRESENIUS/DELMED 90/2 PERITONEAL DIALYSIS SYSTEM

FDA 510(k), K902149, FRESENIUS/DELMED 90/2 PERITONEAL DIALYSIS SYSTEM

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510(K) Number: K902149
Device Name: FRESENIUS/DELMED 90/2 PERITONEAL DIALYSIS SYSTEM
Manufacturer:
Device Classification Name: System, Peritoneal, Automatic Delivery
Regulation Number: 876.5630
Classification Product Code: FKX
Date Received: 05/15/1990
Decision Date: 10/30/1990
Regulation Medical Specialty: Gastroenterology/Urology
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