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510(k) Data Aggregation

    K Number
    K040192

    Validate with FDA (Live)

    Date Cleared
    2004-02-27

    (30 days)

    Product Code
    Regulation Number
    892.5050
    Reference & Predicate Devices
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The On-Board Imager device is used for verification of correct patient position in relation to isocenter and verification of the treatment fields in relation to anatomical and/or fiducial landmarks.

    Device Description

    PortalVision has been modified to add a kilovoltage xray source and digital imaging system to allow for improved image quality. This additional option will be called the On-Board Imager device and its intended use will be to supplement the PortalVision device or be used as a stand-alone device to allow for verification of correct patient position in relation to isocenter and verification of the treatment fields in relation anatomical and/or fiducial landmarks.

    AI/ML Overview

    The provided text is a 510(k) summary for the Varian Medical Systems On-Board Imager, a device intended to verify patient position and treatment fields in relation to anatomical or fiducial landmarks during radiation therapy.

    However, the provided document does not contain any information regarding acceptance criteria or a study that proves the device meets specific performance criteria. The text describes the device, its intended use, and its substantial equivalence to predicate devices but omits details about performance metrics, study designs, sample sizes, ground truth establishment, or expert involvement.

    Therefore, I cannot provide the requested table or answer the specific questions based on the information given. The document focuses on regulatory approval based on substantial equivalence rather than detailed performance study results.

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