WAVELIGHT FS200 PATIENT INTERFACE 1505

WAVELIGHT FS200 PATIENT INTERFACE 1505 is an FDA 510(k)-cleared medical device (K121031) manufactured by Alcon Research, Ltd.. 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 June 20, 2012. Regulation: 8.