
Precision Vascular Systems, Inc.
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PVS 1300 SYNCHRO 0.014 & PVS 1600 SYNCHRO 0.010 GUIDE WIRES is an FDA 510(k)-cleared medical device (K032146) manufactured by Precision Vascular Systems, 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 August 11, 2003. Regulation: 8.