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

    AMX5 AND AMX5D MOBILE X-RAY SYSTEMS

    K Number: K042866 · Decision Nov 2, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    235
    Applicant Total
    2
    Review Days
    15

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    Basic Information

    Device Name
    AMX5 AND AMX5D MOBILE X-RAY SYSTEMS
    K Number
    K042866
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1720
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ge Healthcare Technologies
    Date Received
    October 18, 2004
    Decision Date
    November 2, 2004
    Product Code
    IZL
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    IZL System, X-Ray, Mobile

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    Other Clearances by Ge Healthcare Technologies

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