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FDA 510(k), K043363, FRESENIUS LIBERTY CYCLER
FDA 510(k), K043363, FRESENIUS LIBERTY CYCLER
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510(K) Number: K043363
Device Name: FRESENIUS LIBERTY CYCLER
Manufacturer: FRESENIUS MEDICAL CARE NORTH AMERICA
Device Classification Name: system, peritoneal, automatic delivery
Regulation Number: 876.5630
Classification Product Code: FKX
Date Received: 12/07/2004
Decision Date: 03/31/2005
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: FRESENIUS LIBERTY CYCLER
Manufacturer: FRESENIUS MEDICAL CARE NORTH AMERICA
Device Classification Name: system, peritoneal, automatic delivery
Regulation Number: 876.5630
Classification Product Code: FKX
Date Received: 12/07/2004
Decision Date: 03/31/2005
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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