AIP INTENSE PULSED LIGHT SYSTEM

AIP INTENSE PULSED LIGHT SYSTEM is an FDA 510(k)-cleared medical device (K041554) manufactured by Aesthera Corporation. 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 April 26, 2005. Regulation: 8.