Guidant Corporation
MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM
SKU K032530UPC FGE
In Stock
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IIFDA 510(k) Cleared (K032530)
1
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Guidant Corporation
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM is an FDA 510(k)-cleared medical device (K032530) manufactured by Guidant 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 October 22, 2003. Regulation: 8.
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