ZEBRA UROLOGICAL GUIDEWIRE

ZEBRA UROLOGICAL GUIDEWIRE is an FDA 510(k)-cleared medical device (K942205) manufactured by Boston Scientific Corp. 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 July 6, 1994. Regulation: 8.