DORNIER THERMAFOCUS 360 FIBER

DORNIER THERMAFOCUS 360 FIBER is an FDA 510(k)-cleared medical device (K950996) manufactured by Daimler-Benz Aerospace. 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 October 2, 1995. Regulation: 8.