Cordis Neurovascular, Inc.
MODIFICATION TO HYPERTRANSIT INFUSION CATHETER
SKU K070279UPC KRA
In Stock
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IIFDA 510(k) Cleared (K070279)
1
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Cordis Neurovascular, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO HYPERTRANSIT INFUSION CATHETER is an FDA 510(k)-cleared medical device (K070279) manufactured by Cordis Neurovascular, Inc.. 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 13, 2007. Regulation: 8.
