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Perfuze Secures the US FDA’s 510(k) Clearance for its Zipline Access Catheters

Shots:

  • The US FDA has granted 510(k) clearance to Zipline Access Catheters to treat acute ischemic strokes
  • Zipline improves delivery of a large (070) & superbore (088) aspiration catheter to enhance trackability & simplify neuro-interventional procedures for faster as well as more efficient stroke treatment. Zipline also optimizes clot removal & improves success rates with added support & easy navigation
  • Additionally, Perfuze has secured $23.9M (€22M) from existing investors, incl. Earlybird, EQT Life Sciences, Seroba, & SV Health, to advance clinical and R&D activities, plus to support limited market release of Zipline & Millipede catheters, which are now launched in the US

Ref: BusinessWire | Image: Perfuze

Related News:- Ultromics’ EchoGo Amyloidosis Receives the US FDA’s Breakthrough Device Designation to Detect Cardiac Amyloidosis

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