BD PosiFlush Heparin Lock Flush Syringe

BD PosiFlush Heparin Lock Flush Syringe is an FDA 510(k)-cleared medical device (K163591) 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 February 26, 2017. Regulation: 8.