
Cook Incorporated
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Kwart Retro-Inject Ureteral Stent is an FDA 510(k)-cleared medical device (K162109) manufactured by Cook Incorporated. 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 June 6, 2017. Regulation: 8.