
Boston Scientific Corporation
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UROMAX ULTRA BALLOON DILATATION CATHETER is an FDA 510(k)-cleared medical device (K130804) manufactured by Boston Scientific Corporation. 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 May 21, 2013. Regulation: 8.