GUIDEWIRE, MODEL G-V220-3527S AND OTHERS

GUIDEWIRE, MODEL G-V220-3527S AND OTHERS is an FDA 510(k)-cleared medical device (K072354) manufactured by Accellent, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 2007. Regulation: 8.