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FDA 510(k) K002892, FRSENIUS PD IQCARD CYCLER, by Fresenius Medical Care North America

FDA 510(k) K002892, FRSENIUS PD IQCARD CYCLER, by Fresenius Medical Care North America

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510(K) Number: K002892
Device Name: FRSENIUS PD IQCARD CYCLER
Manufacturer: Fresenius Medical Care North America
Device Classification Name: system, peritoneal, automatic delivery
Regulation Number: 876.5630
Classification Product Code: FKX
Date Received: 09/15/2000
Decision Date: 04/05/2001
Regulation Medical Specialty: Gastroenterology/Urology
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