Guidant Corp.
AGILTRAC .018 PERIPHERAL DILATATION CATHETER
SKU K020161UPC DQY
In Stock
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IIFDA 510(k) Cleared (K020161)
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Free shipping on orders over $99 · 30-day returns
Guidant Corp.
Free shipping on orders over $99 · 30-day returns
AGILTRAC .018 PERIPHERAL DILATATION CATHETER is an FDA 510(k)-cleared medical device (K020161) manufactured by Guidant Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 21, 2002. Regulation: 8.
