MUELLER HINTON AGAR W/HEMOGLOBIN

MUELLER HINTON AGAR W/HEMOGLOBIN is an FDA 510(k)-cleared medical device (K760459) 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 September 2, 1976. Regulation: 8.