CANDIDA BROM CRESOL GREEN AGAR

CANDIDA BROM CRESOL GREEN AGAR is an FDA 510(k)-cleared medical device (K864077) 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 30, 1986. Regulation: 8.