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Js Vascular, Inc.
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JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE is an FDA 510(k)-cleared medical device (K032411) manufactured by Js Vascular, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 6, 2003. Regulation: 8.