BD SoloShot Mini Syringe/ BD Auto Disable Syringe

BD SoloShot Mini Syringe/ BD Auto Disable Syringe is an FDA 510(k)-cleared medical device (K201234) 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 14, 2020. Regulation: 8.