
Continuum Electro-Optics, Inc.
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MEDLITE Q-SWITCHED ND:YAG LASER REPLACED BY THE MEDLITE C3 Q-SWTICHED ND:YAG LASER is an FDA 510(k)-cleared medical device (K011677) manufactured by Continuum Electro-Optics, 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 June 21, 2001. Regulation: 8.