
Applied Optronics Corp.
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AOC MEDICAL SYSTEM MODEL PHASE II 50 SURGICAL DIODE LASER SYSTEM is an FDA 510(k)-cleared medical device (K961705) manufactured by Applied Optronics 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 October 31, 1996. Regulation: 8.