Cordis Corp.
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE
SKU K101651UPC NTE
In Stock
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IIFDA 510(k) Cleared (K101651)
1
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Cordis Corp.
Free shipping on orders over $99 · 30-day returns
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE is an FDA 510(k)-cleared medical device (K101651) 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 July 8, 2010. Regulation: 8.
