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    FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

    Everyway OTC EMS, Model EV-805

    K Number: K162744 · Decision Aug 3, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    161
    Applicant Total
    2
    Review Days
    307

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    Basic Information

    Device Name
    Everyway OTC EMS, Model EV-805
    K Number
    K162744
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5850
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Everyway Medical Instrument Co., Ltd.
    Date Received
    September 30, 2016
    Decision Date
    August 3, 2017
    Product Code
    NGX
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    NGX Stimulator, Muscle, Powered, For Muscle Conditioning

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    Other Clearances by Everyway Medical Instrument Co., Ltd.

    K Number Device Name
    K161349 Everyway Incontinence Stimulation System