BACTEC 9240 SYSTEM

BACTEC 9240 SYSTEM is an FDA 510(k)-cleared medical device (K915796) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 21, 1992. Regulation: 8.