PROGESTERONE RADIOIMMUNOASSAY KIT

PROGESTERONE RADIOIMMUNOASSAY KIT is an FDA 510(k)-cleared medical device (K791051) manufactured by Cis Radiopharmaceuticals, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 23, 1979. Regulation: 8.