Honda Walking Assist Device— 510(k) K181294

Name: FDA 510(k) clearance K181294
Creator: U.S. Food and Drug Administration
Published: 2018-12-14

Substantially Equivalent

Honda Motor Company, Ltd.

FDA 510(k) clearance K181294 for Honda Walking Assist Device, Substantially Equivalent on 2018-12-14. Applicant: Honda Motor Company, Ltd.. Device class: 2.

Clearance details

Applicant: Honda Motor Company, Ltd.
Product code: Code PHL
Device class: Class 2
Regulation: 21 CFR 890.3480
Advisory panel: Physical Medicine
Date received: 2018-05-16
Decision date: 2018-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wako-Shi, JP

Download summary PDF View on FDA.gov ↗

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