HEPARIN LOCK / FLUSH SYRINGES

HEPARIN LOCK / FLUSH SYRINGES is an FDA 510(k)-cleared medical device (K133446) manufactured by Excelsior Medical Corporation. 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 November 13, 2014. Regulation: 8.