PREGELLED DISPOS. ELECTROSURG. GROUND EL

PREGELLED DISPOS. ELECTROSURG. GROUND EL is an FDA 510(k)-cleared medical device (K810277) manufactured by Conmedcorp. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 10, 1981. Regulation: 8.