PVS 1300 NEURO GUIDE WIRE

PVS 1300 NEURO GUIDE WIRE is an FDA 510(k)-cleared medical device (K002907) 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 March 7, 2001. Regulation: 8.