DERMA K ER:YAG/CO2 LASER

DERMA K ER:YAG/CO2 LASER is an FDA 510(k)-cleared medical device (K982827) manufactured by Esc Medical Systems, 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 September 13, 1998. Regulation: 8.