Guidant Corp.
MODIFICATION TO RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005126-13, 1005128-13, 1005130-13, 1005132-13, 1005134-13,
SKU K993588UPC FGE
In Stock
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IIFDA 510(k) Cleared (K993588)
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Free shipping on orders over $99 · 30-day returns
Guidant Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005126-13, 1005128-13, 1005130-13, 1005132-13, 1005134-13, is an FDA 510(k)-cleared medical device (K993588) manufactured by Guidant Corp.. 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 November 16, 1999. Regulation: 8.
