MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP

MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP is an FDA 510(k)-cleared medical device (K895864) manufactured by Lasag AG. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 28, 1989. Regulation: 8.