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510(k) Data Aggregation

    K Number
    K061269
    Manufacturer
    Date Cleared
    2006-08-14

    (101 days)

    Product Code
    Regulation Number
    882.1320
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    XLTEK CLEAN SIGNAL ADHESIVE ELECTRODES

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

    XLTEK Clear Signal Adhesive Electrodes are intended for use with recording, monitoring and stimulation equipment for the purpose of recording of biopotential signals. Examples include: Electromyography (EMG), Electroencephalograph (EEG) and Nerve potential signals. The electrodes are for single patient use only.

    Device Description

    Not Found

    AI/ML Overview

    I am sorry, but the provided text does not contain the information required to describe the acceptance criteria and the study that proves the device meets those criteria. The document is a 510(k) clearance letter from the FDA for "XLTEK Clear Signal Adhesive Electrodes". It confirms that the device is substantially equivalent to legally marketed predicate devices and outlines general regulatory requirements.

    Specifically, the document does not include:

    • A table of acceptance criteria and reported device performance.
    • Details about a study, including sample sizes, data provenance, number or qualifications of experts, adjudication methods, or ground truth establishment.
    • Information on MRMC comparative effectiveness studies or standalone algorithm performance.
    • Details about training sets.

    The document primarily states the device's intended use and confirms its regulatory clearance by the FDA.

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