LEECO PROGESTERONE-QUANT DIAGNOSTIC TEST KIT

LEECO PROGESTERONE-QUANT DIAGNOSTIC TEST KIT is an FDA 510(k)-cleared medical device (K850056) manufactured by Leeco Diagnostics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 5, 1985. Regulation: 8.