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Photo Medex, Inc.
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LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS is an FDA 510(k)-cleared medical device (K082721) manufactured by Photo Medex, Inc.. 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 October 27, 2008. Regulation: 8.