Arbor Endovascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: Willow 12 Guidewire, Willow 24 Guidewire, Willow 18 Guidewire
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arbor Endovascular, LLC Neurology ✕
5 devices