BECTON DICKINSON INTERLINK VIAL ACCESS CANNULA

BECTON DICKINSON INTERLINK VIAL ACCESS CANNULA is an FDA 510(k)-cleared medical device (K924439) 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 February 11, 1993. Regulation: 8.