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

    BENNETT X-RAY ID PLUS

    K Number: K925332 · Decision Nov 27, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    38
    Registration Numbers
    38
    Same Product Code
    17
    Applicant Total
    2
    Review Days
    37

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    Basic Information

    Device Name
    BENNETT X-RAY ID PLUS
    K Number
    K925332
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1640
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Bennett X-Ray Technologies
    Date Received
    October 21, 1992
    Decision Date
    November 27, 1992
    Product Code
    JAC
    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
    JAC System, X-Ray, Film Marking, Radiographic

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