Medtronic, Inc.
DLP Silicone Coronary Artery Ostial Cannulae
SKU K230960UPC DWF
In Stock
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IIFDA 510(k) Cleared (K230960)
1
Free shipping on orders over $99 · 30-day returns
Medtronic, Inc.
Free shipping on orders over $99 · 30-day returns
DLP Silicone Coronary Artery Ostial Cannulae is an FDA 510(k)-cleared medical device (K230960) manufactured by Medtronic, 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 May 3, 2023. Regulation: 8.
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