Cordis Corp., A Johnson & Johnson Co.
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE
SKU K062531UPC NTE
In Stock
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IIFDA 510(k) Cleared (K062531)
1
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Cordis Corp., A Johnson & Johnson Co.
Free shipping on orders over $99 · 30-day returns
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE is an FDA 510(k)-cleared medical device (K062531) manufactured by Cordis Corp., A Johnson & Johnson Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 21, 2006. Regulation: 8.
