
E.I. Dupont DE Nemours & Co., Inc.
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ACA(R) URINE DRUGS OF ABUSE CONTROL, MODIFICATION is an FDA 510(k)-cleared medical device (K911724) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 21, 1991. Regulation: 8.