TISSUELINK BIPOLAR FLOATING BALL DEVICE

TISSUELINK BIPOLAR FLOATING BALL DEVICE is an FDA 510(k)-cleared medical device (K022532) 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 February 11, 2003. Regulation: 8.