AMPLATZ SUPER STIFF GUIDEWIRE

AMPLATZ SUPER STIFF GUIDEWIRE is an FDA 510(k)-cleared medical device (K944959) 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 November 3, 1994. Regulation: 8.