FOLATE/B12 DUO-BEAD RADIOASSAY

FOLATE/B12 DUO-BEAD RADIOASSAY is an FDA 510(k)-cleared medical device (K822241) manufactured by Abbott Laboratories. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 25, 1982. Regulation: 8.