FDA 510(k) Applications Submitted by SUZANNE DENNIS

FDA 510(k) Number Submission Date Device Name Applicant
K010805 03/16/2001 PRISMA SYSTEM GAMBRO RENAL PRODUCTS
K011221 04/20/2001 PRISMA HF 1000 SET, PRISMA HF 1000 PRE-SET GAMBRO RENAL PRODUCTS
K982256 06/26/1998 OUTBOUND DISPOSABLE SYRINGE INFUSER OUTBOUND 2 DISPOSABLE PUMP MCKINLEY, INC.
K103000 10/08/2010 SMART READ BIOLOGICAL TEST PACK STERITEC PRODUCTS MFG. CO., INC.
K003957 12/21/2000 DIACLEAR ULTRAFILTER GAMBRO RENAL PRODUCTS


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