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

    DIAL-A-RAD PORTA RAD TABLE

    K Number: K913425 · Decision Nov 24, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    26
    Applicant Total
    1
    Review Days
    481

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    Basic Information

    Device Name
    DIAL-A-RAD PORTA RAD TABLE
    K Number
    K913425
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1980
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Dial-A-Rad
    Date Received
    August 1, 1991
    Decision Date
    November 24, 1992
    Product Code
    IXQ
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IXQ Table, Radiographic, Stationary Top

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