Everyway Facial MENS— 510(k) K142794

Name: FDA 510(k) clearance K142794
Creator: U.S. Food and Drug Administration
Published: 2015-06-02

Substantially Equivalent

Everyway Medical Instruments Co.,Ltd

FDA 510(k) clearance K142794 for Everyway Facial MENS, Substantially Equivalent on 2015-06-02. Applicant: Everyway Medical Instruments Co.,Ltd. Device class: 2.

Clearance details

Applicant: Everyway Medical Instruments Co.,Ltd
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2014-09-29
Decision date: 2015-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shen Keng Hsiang, Taipei Hsien, TW

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.