BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    BIOFEEDBACK SYSTEM FOR SPEECH DISORDERS

    K Number: K942651 · Decision Oct 19, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    3
    Applicant Total
    1
    Review Days
    503

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    Basic Information

    Device Name
    BIOFEEDBACK SYSTEM FOR SPEECH DISORDERS
    K Number
    K942651
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    874.5840
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Casa Futura Technologies
    Date Received
    June 3, 1994
    Decision Date
    October 19, 1995
    Product Code
    KTH
    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
    KTH Device, Anti-Stammering

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