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510(k) Data Aggregation

    K Number
    K050190
    Device Name
    APOLLO
    Manufacturer
    VILLA SISTEMI MEDICALI S.P.A.
    Date Cleared
    2005-03-25

    (57 days)

    Product Code
    KXJ, IXL, KPW
    Regulation Number
    892.1980
    Why did this record match?
    Product Code :

    KXJ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The indication for use of the APOLLO is: radiology and fluoroscopy investigations when installed in conjunction with adequate image intensifier, image acquisition systems, X-ray generators and X-ray tubes.
    Device Description
    Remote controlled radiology table, collimator and spot film device
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    K Number
    K963905
    Device Name
    RADIOGRAPHIC ITT TABLE
    Manufacturer
    X-RAY TECHNOLOGIES, INC.
    Date Cleared
    1996-11-12

    (43 days)

    Product Code
    KXJ
    Regulation Number
    892.1980
    Why did this record match?
    Product Code :

    KXJ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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    K Number
    K955414
    Device Name
    XRT 400
    Manufacturer
    WUESTEC MEDICAL, INC.
    Date Cleared
    1996-07-24

    (240 days)

    Product Code
    KXJ
    Regulation Number
    892.1980
    Why did this record match?
    Product Code :

    KXJ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question

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