AMERLEX-M PROGESTERONE RADIOIMMUNOASSAY KIT

AMERLEX-M PROGESTERONE RADIOIMMUNOASSAY KIT is an FDA 510(k)-cleared medical device (K864855) manufactured by Amersham Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 24, 1987. Regulation: 8.