PV 1900 SYNCHRO 0.016 GUIDEWIRE

PV 1900 SYNCHRO 0.016 GUIDEWIRE is an FDA 510(k)-cleared medical device (K050964) manufactured by Boston Scientific - Precision Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 12, 2005. Regulation: 8.