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510(k) Data Aggregation

    K Number
    K023147
    Date Cleared
    2002-12-12

    (83 days)

    Product Code
    Regulation Number
    890.1375
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Bortec Biomedical Analog Multiplexed cable Telemetry (AMT) electromyograph is intended for non-invasive use as a research or diagnostic sensing and processing instrument in studies of physiological signals. The AMT is indicated for use with active or passive adult or pediatric subjects in hospitals or clinics under the direction of a health care professional during electromyography, including bio-feedback, evoked potential, kinesiological, nerve conductance and sleep studies.

    Device Description

    Analog Multiplexed cable Telemetry (AMT) electromyograph

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for the Bortec Biomedical, LTD. Analog Multiplexed Cable Telemetry (AMT) Electromyograph. This document is a regulatory approval and does not contain the acceptance criteria or details of a study proving the device meets those criteria, nor does it provide information about AI-specific performance metrics.

    The letter states that the device has been reviewed and determined to be "substantially equivalent" to legally marketed predicate devices. This means that the FDA found the new device to be as safe and effective as a device already on the market, but it does not require the submission of detailed performance studies in the same way a novel device might.

    Therefore, I cannot fulfill your request for the specific information regarding acceptance criteria and performance studies based on the provided input. The document focuses on regulatory compliance and indications for use, not detailed technical performance data or specific study designs.

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