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510(k) Data Aggregation

    K Number
    K980687
    Date Cleared
    1998-05-22

    (88 days)

    Product Code
    Regulation Number
    892.1560
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K964309

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

    Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows.
    Clinical Applications: Opthalmic, Fetal, Abdominal, Adult Cephalic, Cardiac Adult.
    Mode of Operation: B, M, PWD, CWD, Color Doppler, Power (Amplitude) Doppler, Color Velocity Imaging, Combined (B+M, B+M+Color (CVI), B+PW), Harmonic Imaging of tissue, Harmonic Imaging of contrast agents.

    Device Description

    Functionality: No change. Design cleared with K964309 has the ability to perform harmonic imaging of tissue.
    Scientific Concepts: Use of harmonic imaging reduces clutter in the image. Clutter exists in images of difficult to image patients. It therefore follows that reducing clutter if it exists will improve 2D/ B-mode image quality.
    Significant Characteristics of the Modification: This submittal is being done solely for the purpose of allowing FDA to review claims of effectiveness.
    Significant Safety Concerns: None. Harmonic Imaging of tissue is being done today with several systems already the market.

    AI/ML Overview

    The provided text is a 510(k) summary for the HP Sonos 5500 Ultrasound Imaging System with a Harmonic Tissue Imaging Option. It focuses on demonstrating substantial equivalence to predicate devices and describes the intended use and scientific concepts behind the harmonic imaging feature. However, it does not contain any information about acceptance criteria, specific device performance metrics, study designs (sample sizes, data provenance, expert qualifications, adjudication methods), or ground truth establishment.

    Therefore, I cannot fulfill your request for the detailed table and study information because the necessary data is not present in the provided document.

    The document only states:

    • Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body, with Harmonic Imaging of tissue being a "new indication" (N) with this submittal.
    • Scientific Concept: "Use of harmonic imaging reduces clutter in the image. Clutter exists in images of difficult to image patients. It therefore follows that reducing clutter if it exists will improve 2D/ B-mode image quality."
    • Study Type: "This submittal is being done solely for the purpose of allowing FDA to review claims of effectiveness." However, it does not detail how effectiveness was "proven" with specific performance metrics or studies. It relies on the substantial equivalence to predicate devices that already perform harmonic imaging.
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