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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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