FDA 510(k) Application Details - K013448

Device Classification Name	Dialysate Concentrate For Hemodialysis (Liquid Or Powder)   More FDA Info for this Device
510(K) Number	K013448
Device Name	Dialysate Concentrate For Hemodialysis (Liquid Or Powder)
Applicant	GAMBRO RENAL PRODUCTS 1845 MASON AVE. DAYTONA BEACH, FL 32117-5102 US Other 510(k) Applications for this Company
Contact	FEI LAW Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	KPO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/17/2001
Decision Date	01/15/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review