BD PREEFILE NORMAL SALINE FLUSH SYRINGE FLUSH SYRINGE

BD PREEFILE NORMAL SALINE FLUSH SYRINGE FLUSH SYRINGE is an FDA 510(k)-cleared medical device (K982558) manufactured by Bd/Preefil. 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 March 7, 2000. Regulation: 8.