Ev3 Neurovascular
MERIDIAN GUIDEWIRE
SKU K093681UPC DQX
In Stock
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IIFDA 510(k) Cleared (K093681)
1
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Ev3 Neurovascular
Free shipping on orders over $99 · 30-day returns
MERIDIAN GUIDEWIRE is an FDA 510(k)-cleared medical device (K093681) manufactured by Ev3 Neurovascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 2010. Regulation: 8.
