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510(k) Data Aggregation

    K Number
    K993420
    Date Cleared
    2000-07-19

    (281 days)

    Product Code
    Regulation Number
    890.5850
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • . Interferential Current Therapy Modes: Symptomatic relief and management of chronic pain and/or as an adjunctive treatment for the management of post-surgical and post-traumatic pain.
    • Neuro-Muscular Stimulator Modes: Relaxation of muscle spasm, increasing local blood circu-. lation, maintaining or increasing range of motion, preventing or retarding disuse atrophy, muscle re-education, and immediate post-surgical stimulation of calf muscles to prevent venous thrombosis.
    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for the CS3101 Interferential Stimulator. This document does not contain any information regarding acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert qualifications.

    The letter primarily:

    • Acknowledges receipt and review of the 510(k) submission (K993420).
    • States that the device is substantially equivalent to legally marketed predicate devices.
    • Grants permission to market the device subject to general control provisions.
    • Lists the Indications for Use for the CS3101 Interferential Stimulator.

    Therefore, I cannot provide the requested table and study details based on the input text. The information needed to answer your questions would typically be found in the 510(k) submission itself, particularly in the sections describing performance testing and clinical data (if applicable), which are not present in this clearance letter.

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