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Teleflex Says FDA Clears AC3 Range Intra-Aortic Balloon Pump
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Teleflex Says FDA Clears AC3 Range Intra-Aortic Balloon Pump
Apr 1, 2025 6:08 AM

08:41 AM EDT, 04/01/2025 (MT Newswires) -- Teleflex ( TFX ) said Tuesday that the US Food and Drug Administration granted 510(k) clearance for its AC3 Range Intra-Aortic Balloon Pump to provide cardiac support for patients during transport.

The medical device maker said it will begin shipping the AC3 Range IABP to customers in Q2.

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