Ireland

Perfuze Receives FDA 510(k) Clearance for Zipline™ Access Catheters and Secures €22M in Additional Funding

Perfuze has received FDA 510(k) clearance for its Zipline™ Access Catheters, designed to simplify and enhance stroke treatment. The company also secured €22 million in funding to support the Limited Market Release of Zipline™ and Millipede™ catheters, advancing its mission to improve stroke care through innovative neurovascular technologies.

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