B-D INTERLINK SYRINGE CANNULA

B-D INTERLINK SYRINGE CANNULA is an FDA 510(k)-cleared medical device (K920422) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 28, 1992. Regulation: 8.