ARIA II 125 I CORTISOL

ARIA II 125 I CORTISOL is an FDA 510(k)-cleared medical device (K802380) 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 October 30, 1980. Regulation: 8.