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

    EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS.

    K Number: K760604 · Decision Sep 13, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    54
    Registration Numbers
    54
    Same Product Code
    39
    Applicant Total
    2
    Review Days
    5

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    Basic Information

    Device Name
    EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS.
    K Number
    K760604
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1760
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Eureka X-Ray Tube Corp.
    Date Received
    September 8, 1976
    Decision Date
    September 13, 1976
    Product Code
    ITY
    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
    ITY Assembly, Tube Housing, X-Ray, Diagnostic

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    Other Clearances by Eureka X-Ray Tube Corp.

    K Number Device Name
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