Arbor Endovascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: Willow 24 Guidewire, Willow 18 Guidewire, 0.014” Willow Guidewire
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arbor Endovascular, LLC Neurology ✕
4 devices