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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K243756

0.014” Willow Guidewire · Arbor Endovascular, LLC · decided 2025-07-17 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Willow 14 GuidewireUSTA14SU315LArbor Endovascular LLCDQX MOF00850076777111
Willow 14 GuidewireUSTA14SU215LArbor Endovascular LLCDQX MOF00850076777081
Willow 14 GuidewireUSTA14ST215LArbor Endovascular LLCDQX MOF00850076777074
Willow 14 GuidewireUSTA14ST315SArbor Endovascular LLCDQX MOF00850076777043
Willow 14 GuidewireUSTA14SO315SArbor Endovascular LLCDQX MOF00850076777036
Willow 14 GuidewireUSTA14SO215SArbor Endovascular LLCDQX MOF00850076777005
Willow 14 GuidewireUSTA14ST315LArbor Endovascular LLCDQX MOF00850076777104
Willow 14 GuidewireUSTA14SO315LArbor Endovascular LLCDQX MOF00850076777098
Willow 14 GuidewireUSTA14SO215LArbor Endovascular LLCDQX MOF00850076777067
Willow 14 GuidewireUSTA14SU215SArbor Endovascular LLCDQX MOF00850076777029
Willow 14 GuidewireUSTA14SU315LArbor Endovascular LLCDQX MOF00850076777050
Willow 14 GuidewireUSTA14ST215SArbor Endovascular LLCDQX MOF00850076777012