ESC INTENSE PULSED LIGHT SYSTEMS: EPILIGHT AND MULTILIGHT

ESC INTENSE PULSED LIGHT SYSTEMS: EPILIGHT AND MULTILIGHT is an FDA 510(k)-cleared medical device (K994014) manufactured by Esc Medical Systems , Ltd.. 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 23, 2000. Regulation: 8.