NORTEC URETERAL STENT

NORTEC URETERAL STENT is an FDA 510(k)-cleared medical device (K910691) manufactured by North American Sterilization & Packaging Co.. 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 August 14, 1991. Regulation: 8.