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510(k) Data Aggregation

    K Number
    K022896
    Manufacturer
    Date Cleared
    2002-10-03

    (30 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    CSV12 SOFTWARE VIEWER

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

    The intended use of the CSV12 Software Viewer is acceptance, transfer, display, storage, and digital processing of Cypress diagnostic ultrasound images and image manipulation and quantification. No new intended uses are claimed for the modifications.

    The intended use of the CSV12 Software Viewer is for the acceptance, transfer, display, storage, and digital processing of Cypress Diagnostic Ultrasound System images, including image manipulation and quantification.

    Device Description

    This modification is a software-only version of the Acuson Cypress Diagnostic Ultrasound System Image Viewer and is described as the CSV12 Software Viewer.

    The modifications implemented in the CSV12 Viewer Software are to provide off-line image management of ultrasound studies and images on a PC and may be operated independently as a software-only product.

    The CSV12 Software Viewer, when running on a personal computer (PC) duplicates the patient database, study storage, viewing, and quantification capability of the Cypress ultrasound system. This provides clinicians with a simple means of viewing studies off-line. Because it can read the full-resolution R-Theta file formats of the Cypress diagnostic ultrasound images, the CSV12 Software Viewer displays images in real-time without any compression, duplicating the original quality of the images on the Cypress diagnostic ultrasound system.

    AI/ML Overview

    The provided document is a 510(k) summary for a software viewer (CSV12 Software Viewer) and primarily focuses on establishing substantial equivalence to a predicate device. It does not contain information typically found in a study demonstrating how a device meets acceptance criteria for diagnostic performance (e.g., sensitivity, specificity, accuracy).

    Based on the provided text, here's a breakdown of the requested information:

    1. Table of Acceptance Criteria and Reported Device Performance

    This information is not present in the document. The document describes a software viewer that "duplicates the patient database, study storage, viewing, and quantification capability of the Cypress ultrasound system" and "displays images in real-time without any compression, duplicating the original quality of the images on the Cypress diagnostic ultrasound system." The acceptance criteria for such a device would likely focus on functional equivalence (e.g., ability to open and display images, perform measurements accurately compared to the predicate) rather than diagnostic performance metrics like sensitivity or specificity. No specific quantitative performance metrics are provided.

    2. Sample Size Used for the Test Set and Data Provenance

    This information is not present in the document. The filing discusses the software's capabilities but does not detail a formal test set or its provenance.

    3. Number of Experts Used to Establish Ground Truth for the Test Set and Qualifications

    This information is not present in the document. Since there's no mention of a diagnostic performance study, there's no discussion of ground truth establishment by experts.

    4. Adjudication Method for the Test Set

    This information is not present in the document.

    5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

    A MRMC comparative effectiveness study was not done based on the provided document. The filing is for a software viewer and focuses on its functional equivalence, not on improving human reader performance.

    6. Standalone (Algorithm Only Without Human-in-the-Loop Performance) Study

    A standalone performance study focused on diagnostic accuracy is not relevant/not mentioned for this device as it is a viewer. The "standalone" aspect described in the document refers to the software being able to "operate independently as a software-only product" on a PC, duplicating the existing ultrasound system's viewing capabilities, rather than a diagnostic algorithm working independently.

    7. Type of Ground Truth Used

    Ground truth is not applicable/not mentioned in the context of diagnostic performance criteria for this device as described. The focus is on faithful reproduction and functionality of existing images and data.

    8. Sample Size for the Training Set

    This information is not present in the document. As this is a software viewer that replicates existing functionality, a "training set" in the context of an AI/machine learning algorithm is not applicable or discussed.

    9. How the Ground Truth for the Training Set Was Established

    This information is not present in the document. See point 8.

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