FAMILI OF IRIDEX IQ LASER SYSTEMS

FAMILI OF IRIDEX IQ LASER SYSTEMS is an FDA 510(k)-cleared medical device (K071687) manufactured by Iridex 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 August 6, 2008. Regulation: 8.