ARAMIS DERMATLOGIC LASER

ARAMIS DERMATLOGIC LASER is an FDA 510(k)-cleared medical device (K012545) manufactured by Lumedics, 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 November 4, 2001. Regulation: 8.