Cordis Corp.
CORDIS REFLEX STEERABLE GUIDEWIRE
SKU K930091UPC DQX
In Stock
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IIFDA 510(k) Cleared (K930091)
1
Free shipping on orders over $99 · 30-day returns
Cordis Corp.
Free shipping on orders over $99 · 30-day returns
CORDIS REFLEX STEERABLE GUIDEWIRE is an FDA 510(k)-cleared medical device (K930091) 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 April 6, 1993. Regulation: 8.
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