ESPI NON-INSULATED DOUBLE-ACTION GRASPER, #8203

ESPI NON-INSULATED DOUBLE-ACTION GRASPER, #8203 is an FDA 510(k)-cleared medical device (K903602) 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 September 11, 1990. Regulation: 8.