
Intratherapeutics, Inc.
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INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS is an FDA 510(k)-cleared medical device (K011184) manufactured by Intratherapeutics, Inc.. 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 12, 2001. Regulation: 8.

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