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

    RAD II SIMULATOR

    K Number: K834281 · Decision Dec 29, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    69
    Applicant Total
    2
    Review Days
    57

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    Basic Information

    Device Name
    RAD II SIMULATOR
    K Number
    K834281
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.5840
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Haynes Radiation Ltd., Inc.
    Date Received
    November 2, 1983
    Decision Date
    December 29, 1983
    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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    Other Clearances by Haynes Radiation Ltd., Inc.

    K Number Device Name
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