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

    3D ANGIOGRAPHIC IMAGING SYSTEM, MODEL XIDF-100A

    K Number: K002424 · Decision Oct 27, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    145
    Review Days
    80

    Basic Information

    Device Name
    3D ANGIOGRAPHIC IMAGING SYSTEM, MODEL XIDF-100A
    K Number
    K002424
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
    Date Received
    August 8, 2000
    Decision Date
    October 27, 2000
    Product Code
    LLZ
    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
    LLZ System, Image Processing, Radiological

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