BECTON DICKINSON SYRINGSE

BECTON DICKINSON SYRINGSE is an FDA 510(k)-cleared medical device (K954064) 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 November 20, 1995. Regulation: 8.