MODEL 709 BIPOLAR MICRO COAGULATOR

MODEL 709 BIPOLAR MICRO COAGULATOR is an FDA 510(k)-cleared medical device (K863701) manufactured by Bergen Mfg.. 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 October 13, 1986. Regulation: 8.