BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    CONVERSION CONTRACTOR TIMER KIT

    K Number: K791933 · Decision Nov 13, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    42
    Registration Numbers
    42
    Same Product Code
    162
    Applicant Total
    5
    Review Days
    47

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    Basic Information

    Device Name
    CONVERSION CONTRACTOR TIMER KIT
    K Number
    K791933
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1700
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Advanced Instrument Development, Inc.
    Date Received
    September 27, 1979
    Decision Date
    November 13, 1979
    Product Code
    IZO
    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
    IZO Generator, High-Voltage, X-Ray, Diagnostic

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    Other Clearances by Advanced Instrument Development, Inc.

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