BECTON DICKINSON TWINPAK

BECTON DICKINSON TWINPAK is an FDA 510(k)-cleared medical device (K974006) 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 January 21, 1998. Regulation: 8.