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0.014” Willow Guidewire

Arbor Endovascular, LLC · Class II · Cleared Nov 26, 2025

K-numberK253168
Device name0.014” Willow Guidewire
ApplicantArbor Endovascular, LLC
Product codeMOF
Device classClass II
Decision dateNov 26, 2025
DecisionSubstantially Equivalent
Regulation870.1330
AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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