Teleflex Receives FDA 510(k) Clearance for Epidural Catheter

Teleflex has announced it has received FDA 501(k) clearance for its Arrow FlexTip Plus closed tip, multi-port epidural catheter, according to a news release.

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The Arrow FlexTip Plus is designed to help reduce complications commonly associated with epidural catheters, such as vein cannulations and paresthesia.

 

“Teleflex is adding the FlexTip Plus closed tip, multi-port to the Arrow catheter family to continue to support physicians with products that address the concerns anesthesiologists face on a daily basis,” said Cary Vance, president, Teleflex Anesthesia and Respiratory, in the release. “The FlexTip Plus closed tip, multi-port is based on proven technology, helping anesthesiologists achieve the drug dispersion they prefer with the quality of care they demand for their patients.”

 

Teleflex is headquartered in Limerick, Pa.

 

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