CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS

CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS is an FDA 510(k)-cleared medical device (K893754) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 13, 1989. Regulation: 8.