LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE

LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE is an FDA 510(k)-cleared medical device (K991285) manufactured by Aesculap-Meditec North America. 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 July 11, 1999. Regulation: 8.