Cordis Corp.
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER
SKU K993720UPC KNQ
In Stock
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IIFDA 510(k) Cleared (K993720)
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Free shipping on orders over $99 · 30-day returns
Cordis Corp.
Free shipping on orders over $99 · 30-day returns
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER is an FDA 510(k)-cleared medical device (K993720) manufactured by Cordis 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 January 17, 2000. Regulation: 8.
