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Maquet lands FDA and CE Mark wins for larger-volume IAB catheter

Tue, 10/30/2012 - 2:12pm
Mass Device

Maquet Cardiovascular lands FDA clearance for a new version of its Sensation Plus intra-aortic balloon catheter.

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Maquet Cardiovascular landed FDA 510(k) clearance and CE Mark approval in the European Union for a new version of its intra-aortic balloon catheters, the Sensation Plus 7.5Fr 40cc.

The larger-volume fiber optic IAB catheter, designed for smaller patients between 5'0" and 5'4", will be on the market in the U.S. and E.U. in October, according to a press release.

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