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510(k) Data Aggregation

    K Number
    K231167
    Date Cleared
    2023-08-09

    (106 days)

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

    Conductive Silicone Rubber Electrode

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

    Conductive silicone rubber electrode are cutaneous electrodes to be used with legally marketed TENS, EMS or NMES devices. The Conductive silicone rubber electrodes are non-sterile reusable conductive garments that are intended to deliver the pulses generated by the electrotherapy stimulator to the body surface with which they are in contact. These body parts can include the upper limb including wrist and hand, elbow or shoulder, lower limb including hip, knee, leg, ankle and feet, and the back of the neck.

    Device Description

    Conductive Silicone Rubber Electrode

    AI/ML Overview

    This document is an FDA clearance letter for a medical device. It does not contain information about acceptance criteria, device performance studies, sample sizes, expert qualifications, or ground truth establishment. This type of information would typically be found in the device's technical specifications, design validation reports, or clinical study summaries, which are not part of this FDA clearance notification.

    Therefore, I cannot provide the requested information based on the provided text. The document primarily confirms that the FDA has determined the "Conductive Silicone Rubber Electrode" device is substantially equivalent to legally marketed predicate devices.

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