NETILMICIN 30 MCG SENSI DISC

NETILMICIN 30 MCG SENSI DISC is an FDA 510(k)-cleared medical device (K830732) 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 7, 1983. Regulation: 8.