BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    NICOLETONE SYSTEM V32 AMPLIFIER

    K Number: K061908 · Decision Nov 6, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    96
    Registration Numbers
    96
    Same Product Code
    188
    Applicant Total
    2
    Review Days
    124

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    Basic Information

    Device Name
    NICOLETONE SYSTEM V32 AMPLIFIER
    K Number
    K061908
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    882.1400
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Viasys Neuro Care
    Date Received
    July 5, 2006
    Decision Date
    November 6, 2006
    Product Code
    GWQ
    Advisory Committee
    Neurology
    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
    GWQ Full-Montage Standard Electroencephalograph

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    Other Clearances by Viasys Neuro Care

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