Guidant Corp.
MODIFICATION TO VIKING OPTIMA GUIDING CATHETER
SKU K013638UPC DQY
In Stock
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IIFDA 510(k) Cleared (K013638)
1
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Guidant Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO VIKING OPTIMA GUIDING CATHETER is an FDA 510(k)-cleared medical device (K013638) 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 December 3, 2001. Regulation: 8.
