Werewolf RF20000 Controller, FLOW 50 Wand

Werewolf RF20000 Controller, FLOW 50 Wand is an FDA 510(k)-cleared medical device (K162074) manufactured by ArthroCare 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 August 21, 2016. Regulation: 8.