LIGHT AGE Q-CLEAR LASER, MODEL 701-1101

LIGHT AGE Q-CLEAR LASER, MODEL 701-1101 is an FDA 510(k)-cleared medical device (K033259) manufactured by Light Age, Inc.. 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 24, 2004. Regulation: 8.