
Cook Incorporated
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Seidmon Antegrade AQ Stent Set is an FDA 510(k)-cleared medical device (K180216) 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 September 27, 2018. Regulation: 8.