
Epulse Technologies, Inc.
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EPULSE MODEL 2940 ER:ASER ER:YAG LASER SYSTEM is an FDA 510(k)-cleared medical device (K973576) manufactured by Epulse Technologies, 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 December 8, 1997. Regulation: 8.