HEPARIN LOCK FLUSH SYRINGE

HEPARIN LOCK FLUSH SYRINGE is an FDA 510(k)-cleared medical device (K032417) manufactured by Am2 Pat, Inc.. 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 December 22, 2003. Regulation: 8.