
Lasag Medical Lasers
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MICRORUPTOR III SYSTEM, CW ND: YAG LASER COMPONENT is an FDA 510(k)-cleared medical device (K895347) manufactured by Lasag Medical Lasers. 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 1, 1990. Regulation: 8.