
Vascular Solutions, Inc.
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VARI-LASE ENDOVENOUS LASER CONSOLE, MODEL 7500 is an FDA 510(k)-cleared medical device (K062822) manufactured by Vascular Solutions, 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 November 20, 2006. Regulation: 8.