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CAO Group, Inc.
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PILOT DIODE LASER, MODEL 002-00139 is an FDA 510(k)-cleared medical device (K100143) manufactured by CAO Group, 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 August 12, 2010. Regulation: 8.