Uresil Corp.
URESIL GUIDEWIRE
SKU K972582UPC FGE
In Stock
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IIFDA 510(k) Cleared (K972582)
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Free shipping on orders over $99 · 30-day returns
Uresil Corp.
Free shipping on orders over $99 · 30-day returns
URESIL GUIDEWIRE is an FDA 510(k)-cleared medical device (K972582) manufactured by Uresil Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 1997. Regulation: 8.
