NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGY

NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGY is an FDA 510(k)-cleared medical device (K972561) 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 5, 1997. Regulation: 8.