MEDILAS H LASER FIBERS

MEDILAS H LASER FIBERS is an FDA 510(k)-cleared medical device (K123385) manufactured by Dornier Medtech America, 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 December 13, 2012. Regulation: 8.