
Minnesota Laser Corp.
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FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGY is an FDA 510(k)-cleared medical device (K852696) manufactured by Minnesota Laser Corp.. 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 September 18, 1985. Regulation: 8.