125I-ALDOSTERONE RIA DIAG. KIT

125I-ALDOSTERONE RIA DIAG. KIT is an FDA 510(k)-cleared medical device (K781504) manufactured by Abbott Laboratories. 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 November 21, 1978. Regulation: 8.