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510(k) Data Aggregation

    K Number
    K130243
    Date Cleared
    2013-03-01

    (29 days)

    Product Code
    Regulation Number
    892.1560
    Reference & Predicate Devices
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The iLab™ Ultrasound Imaging System is intended for ultrasound examinations of intravascular pathology. Intravascular ultrasound is indicated in patients who are candidates for transluminal interventional procedures such as angioplasty and atherectomy.

    Device Description

    The iLab Ultrasound Imaging System is designed for real time viewing of intravascular anatomies and is intended to be a basic diagnostic tool for imaging and evaluation of patients who are candidates for transluminal procedures.

    AI/ML Overview

    The provided document states that no clinical studies were required for the modified iLab™ Ultrasound Imaging System to support substantial equivalence. Therefore, the device's acceptance criteria and performance are not discussed in the context of clinical studies.

    The document explicitly states:

    • "Summary of Clinical Tests: The modified iLab Ultrasound Imaging System did not require clinical studies to support substantial equivalence."

    Instead, the determination of substantial equivalence was based on non-clinical data, including:

    • Functional/performance testing
    • Interoperability testing
    • Electrical Safety testing

    The document notes that:

    • "Design verification testing demonstrates that the modified device meets the acceptance criteria."

    However, the specific acceptance criteria and the reported device performance from these non-clinical tests are not detailed in the provided text.

    Given this, I cannot provide the information requested in your numbered list, as the study details, sample sizes, expert involvement, and ground truth information are not present for clinical performance.

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