CUSHING BAYONET, INSULATED BIPOLAR FORCEP

CUSHING BAYONET, INSULATED BIPOLAR FORCEP is an FDA 510(k)-cleared medical device (K974595) manufactured by Titan Mfg., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 23, 1998. Regulation: 8.