NCONTACT COAGULATION SYSTEM KIT

NCONTACT COAGULATION SYSTEM KIT is an FDA 510(k)-cleared medical device (K062539) manufactured by Ncontact Surgical, 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 November 30, 2006. Regulation: 8.