ARTHROCARE ENT PLASMA WANDS

ARTHROCARE ENT PLASMA WANDS is an FDA 510(k)-cleared medical device (K033257) manufactured by Arthrocare Corp.. 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 29, 2003. Regulation: 8.