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

    INTEGRATED BRACHYTHERAPY UNIT - DIGITAL

    K Number: K072445 · Decision Sep 14, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    69
    Applicant Total
    27
    Review Days
    15

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    Basic Information

    Device Name
    INTEGRATED BRACHYTHERAPY UNIT - DIGITAL
    K Number
    K072445
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.5840
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Nucletron Corp.
    Date Received
    August 30, 2007
    Decision Date
    September 14, 2007
    Product Code
    KPQ
    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
    KPQ System, Simulation, Radiation Therapy

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