
E.I. Dupont DE Nemours & Co., Inc.
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DU PONT TOBRAMYCIN ASSAY REAGENTS is an FDA 510(k)-cleared medical device (K850058) 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 January 17, 1985. Regulation: 8.