PALOMAR DERMALUX PULSED LIGHT SYSTEM

PALOMAR DERMALUX PULSED LIGHT SYSTEM is an FDA 510(k)-cleared medical device (K010618) manufactured by Palomar. 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 9, 2001. Regulation: 8.