ENTEC REFLEX WAND 55, MODEL E4055-00

ENTEC REFLEX WAND 55, MODEL E4055-00 is an FDA 510(k)-cleared medical device (K000036) 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 3, 2000. Regulation: 8.