LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980

LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980 is an FDA 510(k)-cleared medical device (K040294) 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 May 4, 2004. Regulation: 8.