Cordis Europa, N.V.
CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER
SKU K063563UPC LIT
In Stock
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IIFDA 510(k) Cleared (K063563)
1
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Cordis Europa, N.V.
Free shipping on orders over $99 · 30-day returns
CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER is an FDA 510(k)-cleared medical device (K063563) manufactured by Cordis Europa, N.V.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 6, 2007. Regulation: 8.
