BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

    ViMove2

    K Number: K163150 · Decision Jul 14, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    70
    Registration Numbers
    70
    Same Product Code
    74
    Applicant Total
    2
    Review Days
    247

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    Basic Information

    Device Name
    ViMove2
    K Number
    K163150
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    890.1375
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Dorsavi, Ltd.
    Date Received
    November 9, 2016
    Decision Date
    July 14, 2017
    Product Code
    IKN
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IKN Electromyograph, Diagnostic

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    Other Clearances by Dorsavi, Ltd.

    K Number Device Name
    K142494 ViMove