HelixAR Electrosurgical Generator with Argon Beam Coagulation, HelixAR Mobile Pedestal

HelixAR Electrosurgical Generator with Argon Beam Coagulation, HelixAR Mobile Pedestal is an FDA 510(k)-cleared medical device (K172671) manufactured by Conmed Corporation. 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 October 3, 2017. Regulation: 8.