FDA 510(k) Applications for Medical Device Product Code "CKF"
(Phenylphosphate, Alkaline Phosphatase Or Isoenzymes)

FDA 510(k) Number Applicant Device Name Decision Date
K072142 ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. S40 CLINICAL ANALYZER, S TEST ALP, S TEST AMYLASE, S TEST AST 06/26/2008
K963383 HICHEM DIAGNOSTICS HICHEM ALP/AMP REAGENT KIT 09/23/1996


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