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510(k) Data Aggregation

    K Number
    K092550
    Device Name
    TIGRT IVS
    Manufacturer
    Date Cleared
    2009-12-15

    (118 days)

    Product Code
    Regulation Number
    892.5050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    TIGRT IVS

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    TiGRT IVS is intended to be used in conjunction with Linac and Digital Panel for analyzing the current patient position and calculating the patient positioning shift correction factor, as well as the treatment portal verification and record.

    Device Description

    TiGRT IVS is intended to be used in conjunction with Linac and Digital Panel for analyzing the current patient position and calculating the patient positioning shift correction factor, as well as the treatment portal verification and record.

    AI/ML Overview

    The provided text does not contain any information about acceptance criteria or a study proving the device meets acceptance criteria.

    The document is a 510(k) premarket notification for an image viewing system called TiGRT IVS. It primarily focuses on demonstrating substantial equivalence to a predicate device (ExacTrac K072046) based on intended use, design, and performance characteristics.

    Here's what the document does include:

    • Device Name: TiGRT IVS
    • Intended Use: To be used in conjunction with Linac and Digital Panel for analyzing the current patient position, calculating patient positioning shift correction factor, and for treatment portal verification and record.
    • Predicate Device: ExacTrac (K072046)
    • Classification: Class II device (21 CFR 892.5050)
    • Comparison with Predicate Device: A table comparing characteristics like operating system, networking, intended use, application, and DICOM compatibility. All characteristics are either identical or considered substantially equivalent.

    Therefore, I cannot provide the requested information in the table format because the source text does not contain it. This type of document (a 510(k) summary) focuses on substantial equivalence rather than explicit performance data against acceptance criteria.

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