PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE

PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE is an FDA 510(k)-cleared medical device (K023700) 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 December 3, 2002. Regulation: 8.