KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT

KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT is an FDA 510(k)-cleared medical device (K890573) manufactured by Kenlor Industries, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 23, 1989. Regulation: 8.