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510(k) Data Aggregation

    K Number
    K131045
    Date Cleared
    2013-05-29

    (44 days)

    Product Code
    Regulation Number
    870.1425
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ENTERPRISE ECG ANALYSIS / INTERPRETATION SOFTWARE

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

    The "Enterprise ECG Analysis / Interpretation Software" is a tool used by qualified medical professionals to assist with the assessment of arrhythmias using ambulatory EGG data. The software supports downloading and analyzing data recorded in compatible formats from devices used for arrhythmia diagnostics such as Holter, Event Monitor, ambulatory or resting EGG devices, or other similar devices when assessment of the rhythm is necessary. The software can be electronically interfaced, and perform analysis with data transferred from other computer based EGG systems, such as an EGG management system. The software provides EGG signal processing and analysis on a beat by beat basis. ORS and Ventricular Ectopic Beat detection, QRS feature extraction, interval measurement, heart rate measurement, and rhythm analysis for the captured data. The software is not for use in life supporting or life sustaining systems or EGG Alarm devices. The software can be integrated into computerized EGG monitoring devices. In this case the medical device manufacturer will identify the indication for use depending on the application of their device. Analysis metrics are provided in a report which is available for clinician review and printing. The reported ECG metrics include beat by beat heart rate measurement and rhythm analysis. The report does not contain diagnostic interpretation; the reported analysis is provided for review by the care provider to render a diagnosis based on clinical judgment and experience.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) premarket notification for a medical device called "Enterprise ECG Analysis / Interpretation Software." It includes an Indications for Use section (Section 4) but does not contain information about acceptance criteria, study details, or performance metrics. Therefore, I cannot provide the requested information.

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