Perfuze Announces FDA Clearance and First U.S. Clinical Use of Millipede 088 Access Catheter.
Galway, Ireland. 16 February 2023. Perfuze, a medical device company developing next-generation catheter-based technology to treat acute ischemic stroke, has secured its first product clearance from the U.S. Food and Drug Administration (FDA) for the company’s Millipede 088 Access Catheter. The first U.S. clinical procedures with Millipede 088 were successfully performed by physicians at Stony …