ESPI MICRO GRASPER,DOUBLE-ACTION,INSULATED,#8250-N

ESPI MICRO GRASPER,DOUBLE-ACTION,INSULATED,#8250-N is an FDA 510(k)-cleared medical device (K903600) manufactured by Dixon Medical, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 16, 1990. Regulation: 8.