GENICON BIPOLAR FORCEPS MODEL # 600-005-005

GENICON BIPOLAR FORCEPS MODEL # 600-005-005 is an FDA 510(k)-cleared medical device (K041968) manufactured by Genicon. 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 November 2, 2004. Regulation: 8.