VISAGE COSMETIC SURGERY, MODEL V5000

VISAGE COSMETIC SURGERY, MODEL V5000 is an FDA 510(k)-cleared medical device (K992180) 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 March 19, 2000. Regulation: 8.