
E.I. Dupont DE Nemours & Co., Inc.
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DUPONT PHENOBARBITAL ASSAY is an FDA 510(k)-cleared medical device (K860304) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 27, 1986. Regulation: 8.