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510(k) Data Aggregation

    K Number
    K965065
    Device Name
    TECA. MILLENNIUM
    Manufacturer
    Date Cleared
    1997-06-20

    (184 days)

    Product Code
    Regulation Number
    882.1870
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    TECA. MILLENNIUM

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

    The Millennium is a 2 or 5 channel electromyograph which provides facilities for ENG and Evoked Potentials testing for a range of clinical applications. Millennium is designed to enable reliable recording, display and documentation of electrophysiological information from the human nervous and muscular system in a clinical environment.

    Device Description

    The Millennium is a 2 or 5 channel electromyograph which provides facilities for ENG and Evoked Potentials testing for a range of clinical applications.

    AI/ML Overview

    This looks like a 510(k) clearance letter for the Medelec Millennium device, indicating that it is substantially equivalent to previously marketed devices. However, the provided document does not contain any information regarding acceptance criteria, performance studies, sample sizes, ground truth establishment, or expert qualifications.

    The letter is a regulatory approval document and typically refers to information submitted by the manufacturer in their 510(k) application. To answer your questions, I would need to see the actual performance study details submitted with that application, which are not present in the provided text.

    Therefore, I cannot populate the table or answer the specific questions about the study that proves the device meets acceptance criteria.

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