DORNIER MEDILAS D SKINPULSE

DORNIER MEDILAS D SKINPULSE is an FDA 510(k)-cleared medical device (K000072) 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 11, 2000. Regulation: 8.