MINITECK ENTERIC BROTH & ENTEROBACTER

MINITECK ENTERIC BROTH & ENTEROBACTER is an FDA 510(k)-cleared medical device (K812286) 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 October 1, 1981. Regulation: 8.