Cordis Corp.
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
SKU K112797UPC LIT
In Stock
—
IIFDA 510(k) Cleared (K112797)
1
Free shipping on orders over $99 · 30-day returns
Cordis Corp.
Free shipping on orders over $99 · 30-day returns
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER is an FDA 510(k)-cleared medical device (K112797) 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 May 3, 2012. Regulation: 8.
