0.014 Willow Guidewire
K-Number: K243756 · 2025-07-17
ApplicantArbor Endovascular, LLC
Decision Date2025-07-17
Product CodeMOF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
0.014 Willow Guidewire is a medical device manufactured by Arbor Endovascular, LLC. It received FDA 510(k) clearance on 2025-07-17 under approval number K243756. The device is classified under product code MOF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the 0.014 Willow Guidewire?
0.014 Willow Guidewire is a medical device that received FDA 510(k) clearance on 2025-07-17. It is manufactured by Arbor Endovascular, LLC. The 510(k) number is K243756.
When was 0.014 Willow Guidewire approved by the FDA?
0.014 Willow Guidewire received FDA 510(k) clearance on 2025-07-17, under approval number K243756.
What company makes 0.014 Willow Guidewire?
0.014 Willow Guidewire is manufactured by Arbor Endovascular, LLC.
What is the FDA product code for 0.014 Willow Guidewire?
The FDA product code for 0.014 Willow Guidewire is MOF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.