Cordis Corporation
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
SKU K121442UPC LIT
In Stock
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IIFDA 510(k) Cleared (K121442)
1
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Cordis Corporation
Free shipping on orders over $99 · 30-day returns
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER is an FDA 510(k)-cleared medical device (K121442) manufactured by Cordis Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 13, 2012. Regulation: 8.
