BD Plastipak™ Syringe

BD Plastipak™ Syringe is an FDA 510(k)-cleared medical device (K251350) manufactured by Becton, Dickinson and Company. 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 July 28, 2025. Regulation: 8.