BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    TINNITUS THERAPY SYSTEM ANM T30 CR

    K Number: K112752 · Decision Dec 16, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    32
    Registration Numbers
    32
    Same Product Code
    76
    Applicant Total
    1
    Review Days
    86

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    Basic Information

    Device Name
    TINNITUS THERAPY SYSTEM ANM T30 CR
    K Number
    K112752
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.3400
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Anm Adaptive Neuromodulation GmbH
    Date Received
    September 21, 2011
    Decision Date
    December 16, 2011
    Product Code
    KLW
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KLW Masker, Tinnitus

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