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

    CR MAMMOGRAPHY SYSTEM WITH DX-M DIGITIZER

    K Number: K111324 · Decision Dec 22, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    40
    Registration Numbers
    40
    Same Product Code
    54
    Applicant Total
    27
    Review Days
    225

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    Basic Information

    Device Name
    CR MAMMOGRAPHY SYSTEM WITH DX-M DIGITIZER
    K Number
    K111324
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1715
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Agfa Healthcare N.V.
    Date Received
    May 11, 2011
    Decision Date
    December 22, 2011
    Product Code
    MUE
    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
    MUE Full Field Digital, System, X-Ray, Mammographic

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