IMMULITE/IMMULITE 1000 PROGESTERONE CALIBRATION VERIFICATION (CVM)

IMMULITE/IMMULITE 1000 PROGESTERONE CALIBRATION VERIFICATION (CVM) is an FDA 510(k)-cleared medical device (K103683) manufactured by Siemens Healthcare Diagnostics. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 27, 2011. Regulation: 8.