Cardiac Assist, Maquet Cardiovascular, LLC
CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP
SKU K112372UPC DSP
In Stock
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IIFDA 510(k) Cleared (K112372)
1
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Cardiac Assist, Maquet Cardiovascular, LLC
Free shipping on orders over $99 · 30-day returns
CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP is an FDA 510(k)-cleared medical device (K112372) manufactured by Cardiac Assist, Maquet Cardiovascular, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 14, 2011. Regulation: 8.
