
Cj Laser Corp.
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MODEL MM-2405 AND MM-2410 COPPER VAPOR LASER is an FDA 510(k)-cleared medical device (K921298) manufactured by Cj 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 July 1, 1992. Regulation: 8.