
Excel Tech. , Ltd.
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EXCEL DUOPULSE MODEL 3000 COMBINATION HO/ER:YAG is an FDA 510(k)-cleared medical device (K922375) 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 July 7, 1992. Regulation: 8.