BECTON DICKINSON INTERLINK(TM) LEVER/Y LOCK

BECTON DICKINSON INTERLINK(TM) LEVER/Y LOCK is an FDA 510(k)-cleared medical device (K940697) 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 August 29, 1994. Regulation: 8.