CYCLIC AMP RADIOIMMUNOASSAY KIT [125I]

CYCLIC AMP RADIOIMMUNOASSAY KIT [125I] is an FDA 510(k)-cleared medical device (K811273) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 26, 1981. Regulation: 8.