BEUDAMED
    FDA PMA FDA Class 2 Approved 🇺🇸 United States

    Full Field Digital, System, X-Ray, Mammographic

    PMA: P010025 · Supplement: S003 · Decision Oct 10, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    40
    Registration Numbers
    40

    Basic Information

    Device Name
    Full Field Digital, System, X-Ray, Mammographic
    Trade Name
    SELENIA FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM
    PMA Number
    P010025
    Supplement Number
    S003
    Device Class
    FDA Class 2
    Product Code
    MUE
    Generic Name
    Full field digital, system, x-ray, mammographic
    Regulation Number
    892.1715
    Medical Specialty
    Radiology
    Advisory Committee
    Radiology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    October 10, 2003
    Date Received
    April 15, 2003
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE FOLLOWING USER ENHANCEMENTS AND COMPONENTS; AN ADDITIONAL PERIPHERAL CONTRAST ENHANCEMENT (PCE) BASED IMAGE PROCESSING MECHANISM; THE ADDITION OF A HIGH RESOLUTION FUJI FM-DP L IMAGE PRINTER; AND UPDATED LABELING CHANGES FOR THE SELENIA FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM (FFDM).

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MUE Full Field Digital, System, X-Ray, Mammographic