On January 22, 2007 Vascular Solutions, Inc. announced that it had received 510(k) clearance from the U.S. Food & Drug Administration to launch the new 023 version of its Twin-Pass® dual access catheter. The original Twin-Pass catheter was launched in January 2006 as a two lumen catheter designed to be used in conjunction with steerable guidewires to access discrete regions of the coronary and peripheral arterial vasculature. The new 023 version features a larger 0.023” lumen that allows the Twin Pass 023 catheter to measure intra-arterial pressures and deliver specialty guidewires into the distal vasculature. A copy of the press release is furnished as Exhibit 99.1 to this Report.

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