
Laser Media
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FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEM is an FDA 510(k)-cleared medical device (K855197) 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 January 20, 1986. Regulation: 8.