Cordis Corp.
CORDIS TRAPEASE PERMANENT VENA CAVA FILTER WITH THE VISEASE ANGIOGRAPHIC VESSEL DILATOR; MODELS 466-P306AU & 466-P306BU
SKU K020316UPC DQO
In Stock
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IIFDA 510(k) Cleared (K020316)
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Free shipping on orders over $99 · 30-day returns
Cordis Corp.
Free shipping on orders over $99 · 30-day returns
CORDIS TRAPEASE PERMANENT VENA CAVA FILTER WITH THE VISEASE ANGIOGRAPHIC VESSEL DILATOR; MODELS 466-P306AU & 466-P306BU is an FDA 510(k)-cleared medical device (K020316) manufactured by Cordis 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 March 19, 2002. Regulation: 8.
