Medtronic, Inc.
DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF
SKU K123762UPC DWF
In Stock
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IIFDA 510(k) Cleared (K123762)
1
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Medtronic, Inc.
Free shipping on orders over $99 · 30-day returns
DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF is an FDA 510(k)-cleared medical device (K123762) 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 March 26, 2013. Regulation: 8.
