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

    SUPERMAX AUTOMATIC X-RAY PROCESSOR

    K Number: K760905 · Decision Nov 19, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    82
    Applicant Total
    254
    Review Days
    24

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    Basic Information

    Device Name
    SUPERMAX AUTOMATIC X-RAY PROCESSOR
    K Number
    K760905
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1900
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    General Electric Co.
    Date Received
    October 26, 1976
    Decision Date
    November 19, 1976
    Product Code
    IXW
    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
    IXW Processor, Radiographic-Film, Automatic

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