FDA 510(k), K051187, REXEED SERIES DIALYZERS
FDA 510(k), K051187, REXEED SERIES DIALYZERS
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510(K) Number: K051187
Device Name: REXEED SERIES DIALYZERS
Manufacturer: ASAHI KASEI MEDICAL CO., LTD.
Device Classification Name: Dialyzer, High Permeability With Or Without Sealed Dialysate System
Regulation Number: 876.5860
Classification Product Code: KDI
Date Received: 05/09/2005
Decision Date: 06/08/2005
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: REXEED SERIES DIALYZERS
Manufacturer: ASAHI KASEI MEDICAL CO., LTD.
Device Classification Name: Dialyzer, High Permeability With Or Without Sealed Dialysate System
Regulation Number: 876.5860
Classification Product Code: KDI
Date Received: 05/09/2005
Decision Date: 06/08/2005
Regulation Medical Specialty: Gastroenterology/Urology
- 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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