Cordis Corp.
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER
SKU K023907UPC KNQ
In Stock
—
IIFDA 510(k) Cleared (K023907)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Cordis Corp.
Free shipping on orders over $99 · 30-day returns
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER is an FDA 510(k)-cleared medical device (K023907) 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 December 17, 2002. Regulation: 8.
Coloplast
SKU MSC612995
Karl Storz Endoscopy
SKU K942112
Coloplast
SKU MSC750215
Coloplast
SKU MSC891872