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FDA 510(k) Applications for Medical Device Product Code "CKF"
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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 |