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

    MAICO MB 11 WITH BERAPHONE PROBE

    K Number: K082035 · Decision Jan 29, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    57
    Registration Numbers
    57
    Same Product Code
    75
    Applicant Total
    1
    Review Days
    196

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    Basic Information

    Device Name
    MAICO MB 11 WITH BERAPHONE PROBE
    K Number
    K082035
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1900
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Maico Diagnostics
    Date Received
    July 17, 2008
    Decision Date
    January 29, 2009
    Product Code
    GWJ
    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
    GWJ Stimulator, Auditory, Evoked Response

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