Cardeon Corp.
MODIFICATION TO CARDEON AEGIS CATHETER
SKU K022174UPC DWF
In Stock
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IIFDA 510(k) Cleared (K022174)
1
Free shipping on orders over $99 · 30-day returns
Cardeon Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO CARDEON AEGIS CATHETER is an FDA 510(k)-cleared medical device (K022174) manufactured by Cardeon 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 July 28, 2002. Regulation: 8.
