LEUCOPREP BRAND TUBE

LEUCOPREP BRAND TUBE is an FDA 510(k)-cleared medical device (K872775) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 1, 1987. Regulation: 8.