VARI-LASE WIREFIBER LASER FIBER

VARI-LASE WIREFIBER LASER FIBER is an FDA 510(k)-cleared medical device (K113140) 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 December 21, 2011. Regulation: 8.