MODIFICATION TO URETERAL STENT

MODIFICATION TO URETERAL STENT is an FDA 510(k)-cleared medical device (K040760) manufactured by Applied Medical Resources 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 October 14, 2004. Regulation: 8.