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510(k) Data Aggregation

K Number

Device Name

0.014 Willow Guidewire

Manufacturer

Arbor Endovascular, LLC

Date Cleared

2025-07-17

(223 days)

Product Code

MOF

Regulation Number

870.1330

Why did this record match?

Applicant Name (Manufacturer) :

Arbor Endovascular, LLC

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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