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FDA 510(k), K123835, 2008 HEMODIALYSIS SORBENT SYSTEM
FDA 510(k), K123835, 2008 HEMODIALYSIS SORBENT SYSTEM
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510(K) Number: K123835
Device Name: 2008 HEMODIALYSIS SORBENT SYSTEM
Manufacturer: DAVID VANELLA
Device Classification Name: System, Dialysate Delivery, Sorbent Regenerated
Regulation Number: FKT
Classification Product Code: KXA
Date Received: 12/13/2012
Decision Date: 02/15/2013
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: 2008 HEMODIALYSIS SORBENT SYSTEM
Manufacturer: DAVID VANELLA
Device Classification Name: System, Dialysate Delivery, Sorbent Regenerated
Regulation Number: FKT
Classification Product Code: KXA
Date Received: 12/13/2012
Decision Date: 02/15/2013
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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