BIO-RAD MICROPLATE 17-HYDROXYPROGESTERONE TEST

BIO-RAD MICROPLATE 17-HYDROXYPROGESTERONE TEST is an FDA 510(k)-cleared medical device (K973350) manufactured by Bio-Rad. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 8, 1998. Regulation: 8.