0.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush Syringe

0.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush Syringe is an FDA 510(k)-cleared medical device (K231161) 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 20, 2023. Regulation: 8.