MONOJECT 512 SYRINGES W/WO NEEDLES

MONOJECT 512 SYRINGES W/WO NEEDLES is an FDA 510(k)-cleared medical device (K820716) manufactured by Sherwood Medical Co.. 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 April 13, 1982. Regulation: 8.