DORNIER MEDILAS H30 SOLVO

DORNIER MEDILAS H30 SOLVO is an FDA 510(k)-cleared medical device (K122159) 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 January 31, 2013. Regulation: 8.