10:57 AM EDT, 07/31/2024 (MT Newswires) -- Teleflex ( TFX ) said Wednesday it received the US Food and Drug Administration's 510(k) clearance for its Ringer perfusion balloon catheter, expanding its interventional cardiology portfolio.

The product will enter a limited market release phase in August, the company said.

Teleflex ( TFX ) shares were down 1% in recent trading.

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