
Coherent Medical Group
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COHERENT VERSAPULSE(TM) 2.1XE/2.1L HOLMI SURG LASE is an FDA 510(k)-cleared medical device (K914136) manufactured by Coherent Medical Group. 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 20, 1992. Regulation: 8.