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510(k) Data Aggregation

    K Number
    K091856
    Manufacturer
    Date Cleared
    2009-08-07

    (45 days)

    Product Code
    Regulation Number
    870.2360
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The ConMed" ECG Monitoring Electrodes are pre-gelled, single patient use, disposable electrocardiographic electrodes for use as an accessory to ECG equipment for long term or short term monitoring and diagnostic procedures with regular or diaphoretic adhesives.

    Device Description

    Not Found

    AI/ML Overview

    This document is a 510(k) summary for the ConMed™ ECG Monitoring Electrodes. It describes the device, its intended use, and its substantial equivalence to previously marketed predicate devices. However, this document does not contain any information about acceptance criteria or a study proving the device meets those criteria, nor does it include information about performance data or ground truth establishment relevant to an AI/algorithm-based device study.

    Therefore, I cannot provide the requested information based on the provided text. The document is a regulatory submission for a physical medical device (electrodes), not a software or AI-powered device that would typically undergo the kind of performance studies and ground truth establishment you are asking about.

    The questions you've posed are appropriate for evaluating an AI/algorithm-driven medical device, but they are not applicable to the traditional medical device described in this 510(k) submission.

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