FDA 510(k) Applications for Medical Device Product Code "CKE"
(Acid Phosphatase, Thymolphthale Inmonophosphate)

FDA 510(k) Number Applicant Device Name Decision Date
K821526 ANCO MEDICAL REAGENTS & ASSOC. ACID PHOSPHATASE REAGENT SET 06/10/1982
K790524 DATA MEDICAL ASSOCIATES, INC. DATA-ZYME ACIA PHOSPHATASE PROCEDURE 05/23/1979
K843380 DIAGNOSTIC CHEMICALS, LTD. (USA) ACID PHOSPHATASE ASSAY KIT 09/20/1984
K864230 E.I. DUPONT DE NEMOURS & CO., INC. DIMENSION (TM) CLINICAL CHEMISTRY SYSTEM 11/28/1986
K914167 EASTMAN KODAK COMPANY CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE 03/17/1992
K873726 KING DIAGNOSTICS, INC. ACID PHOSPHATASE TEST 01/27/1988
K800693 STANBIO LABORATORY STANBIO PROSTATIC ACID PHOSPHATASE TEST 04/16/1980
K860476 STERLING DIAGNOSTICS, INC. ACID PHOSPHATASE REAGENT SET 03/05/1986
K915705 TECH INTL. CO. ACID PHOSPHATASE REAGENT SET 02/27/1992


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