FDA Clears Teleflex’s ARROW Triple Hemodialysis Catheter

The FDA has granted 510(k) clearance to Teleflex for its ARROW Triple lumen pressure injectable acute hemodialysis catheter.

According to the company, the catheter provides maximal barrier protection against infections while helping hospitals maintain compliance with vascular access guidelines and standards. It is available with Teleflex’s ARROW ErgoPack System.

Headquartered in Wayne, Pa., Teleflex specializes in products and services for vascular access, respiratory care, general and regional anesthesia, cardiac care, urology and surgery. — Michael Cipriano