KAVO K.E.Y. LASER 1242

KAVO K.E.Y. LASER 1242 is an FDA 510(k)-cleared medical device (K000805) manufactured by Kavo America. 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 May 3, 2000. Regulation: 8.