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FDA 510(k), K043574, ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
FDA 510(k), K043574, ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
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510(K) Number: K043574
Device Name: ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
Manufacturer: RICHARD CONFER
Device Classification Name: System, Dialysate Delivery, Sorbent Regenerated
Regulation Number: FKT
Classification Product Code: 12/27/2004
Date Received: 06/03/2005
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
Manufacturer: RICHARD CONFER
Device Classification Name: System, Dialysate Delivery, Sorbent Regenerated
Regulation Number: FKT
Classification Product Code: 12/27/2004
Date Received: 06/03/2005
Decision Date: Substantially Equivalent (SESE)
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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