
Boston Scientific Corp
Free shipping on orders over $99 · 30-day returns
MODIFIED URETERAL INDWELLING CATHETER/STENT is an FDA 510(k)-cleared medical device (K974541) 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 February 8, 1998. Regulation: 8.