CINOXACIN 100 MCG SENSI DISC

CINOXACIN 100 MCG SENSI DISC is an FDA 510(k)-cleared medical device (K800540) 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 April 1, 1980. Regulation: 8.