
E.I. Dupont DE Nemours & Co., Inc.
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TIBC PRETREATMENT KIT is an FDA 510(k)-cleared medical device (K842019) 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 June 21, 1984. Regulation: 8.