KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ is an FDA 510(k)-cleared medical device (K030146) 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 August 2, 2005. Regulation: 8.