PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH

PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH is an FDA 510(k)-cleared medical device (K873431) manufactured by Serono Diagnostics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 19, 1987. Regulation: 8.