REAGENT SYSTEM, PROGESTERONE, ARIA

REAGENT SYSTEM, PROGESTERONE, ARIA is an FDA 510(k)-cleared medical device (K770732) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1977. Regulation: 8.