
American Laser Medical
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NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER is an FDA 510(k)-cleared medical device (K972765) manufactured by American Laser Medical. 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 20, 1997. Regulation: 8.