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Arthrocare Corp.
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ENTEC CONTROLLER, ENTEC PATIENT CABLE, FOOTSWITCH, POWERCORD, PLASMA WAND is an FDA 510(k)-cleared medical device (K000228) 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 February 21, 2000. Regulation: 8.