EXCEL DUOPAULSE MODEL 2000

EXCEL DUOPAULSE MODEL 2000 is an FDA 510(k)-cleared medical device (K915679) manufactured by Excel Tech. , Ltd.. 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 23, 1992. Regulation: 8.