ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY

ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY is an FDA 510(k)-cleared medical device (K831826) manufactured by Damon Corp.. 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 July 17, 1983. Regulation: 8.