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

    NORELCO VIBRATING BOARD V900

    K Number: K830715 · Decision May 25, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    64
    Applicant Total
    15
    Review Days
    77

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    Basic Information

    Device Name
    NORELCO VIBRATING BOARD V900
    K Number
    K830715
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5975
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    North American Philips Corp.
    Date Received
    March 9, 1983
    Decision Date
    May 25, 1983
    Product Code
    IRO
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IRO Vibrator, Therapeutic

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