DORNIER LASERTRODE FIBER

DORNIER LASERTRODE FIBER is an FDA 510(k)-cleared medical device (K991183) manufactured by Dornier Surgical Products, Inc.. 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 8, 1999. Regulation: 8.