FDA 510(k) Applications for Medical Device Product Code "CDF"
(Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin)

FDA 510(k) Number Applicant Device Name Decision Date
K953077 BECKMAN INSTRUMENTS, INC. PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM 01/05/1996
K873372 BIO-RAD HVA & HOMOVANILLIC ACID BY HPLC METHOD 12/22/1987
K791837 BIO-RAD VMA BY COLUMN TEST 10/30/1979
K861010 BIO-RAD VMA BY HPLC TEST (VANILMANDELIC ACID) 05/01/1986
K843379 DIAGNOSTIC CHEMICALS, LTD. (USA) VMA ASSAY KIT 09/28/1984
K772151 EPPENDORF-BRINKMANN, INC. URINARY VMA - SCREEN TEST KIT 11/30/1977
K934977 ESA, INC. MODEL 5500 CEAS 01/11/1994
K853041 GERMAN AMERICAN CHAMBER OF COMMERCE, INC. TRIGLYCERIDES LCK 124 08/12/1985
K810992 HELENA LABORATORIES HELENA VMA-SMC COLUMN METHOD 04/29/1981
K861962 STERLING DIAGNOSTICS, INC. VANILMANDELIC ACID (VMA) REAGENT SET 07/07/1986
K895288 YAMASA SHOY CO., LTD. HVA EIA KIT YAMASA 10/31/1989
K895287 YAMASA SHOY CO., LTD. VMA EIA KIT YAMASA 10/30/1989


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