FDA 510(k) Applications Submitted by GAMBRO RENAL CARE PRODUCTS

FDA 510(k) Number Submission Date Device Name Applicant
K030592 02/25/2003 GAMBRO POLYFLUX, MODEL 140H, 170H, 210H GAMBRO RENAL CARE PRODUCTS
K993064 09/13/1999 PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM) GAMBRO RENAL CARE PRODUCTS


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