TISSUELINK BIPOLAR FORCEPS

TISSUELINK BIPOLAR FORCEPS is an FDA 510(k)-cleared medical device (K003005) manufactured by Tissuelink Medical, Inc.. 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 December 7, 2000. Regulation: 8.