BD Hypodermic Syringe

BD Hypodermic Syringe is an FDA 510(k)-cleared medical device (K203453) 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 January 24, 2021. Regulation: 8.