
E.I. Dupont DE Nemours & Co., Inc.
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DUPONT 'ACA' CREATINE KINASE VERIFIERS is an FDA 510(k)-cleared medical device (K803305) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 15, 1981. Regulation: 8.