EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908— 510(k) K110509

Name: FDA 510(k) clearance K110509
Creator: U.S. Food and Drug Administration
Published: 2011-06-20

Substantially Equivalent

Everyway Medical Instruments Co.,Ltd

FDA 510(k) clearance K110509 for EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908, Substantially Equivalent on 2011-06-20. Applicant: Everyway Medical Instruments Co.,Ltd. Device class: 2.

Clearance details

Applicant: Everyway Medical Instruments Co.,Ltd
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2011-02-22
Decision date: 2011-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Roswell, GA, US

Download summary PDF View on FDA.gov ↗

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