FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE

FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE is an FDA 510(k)-cleared medical device (K872350) manufactured by Laser Media. 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 9, 1987. Regulation: 8.