MEDILAS D FAMILY LASERS

MEDILAS D FAMILY LASERS is an FDA 510(k)-cleared medical device (K070536) 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 May 20, 2007. Regulation: 8.