CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER

CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER is an FDA 510(k)-cleared medical device (K863583) manufactured by Laser Media. 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 23, 1986. Regulation: 8.