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    FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

    4 CHANNELS MULTIPLE MODEL DIGITAL ELECTRICAL STIMULATOR, MODEL NUVOSTIM IV, WL-2504A

    K Number: K100399 · Decision Jun 25, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    184
    Registration Numbers
    184
    Same Product Code
    605
    Applicant Total
    22
    Review Days
    129

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    Basic Information

    Device Name
    4 CHANNELS MULTIPLE MODEL DIGITAL ELECTRICAL STIMULATOR, MODEL NUVOSTIM IV, WL-2504A
    K Number
    K100399
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    882.5890
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Well-Life Healthcare Limited
    Date Received
    February 16, 2010
    Decision Date
    June 25, 2010
    Product Code
    GZJ
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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    Other Clearances by Well-Life Healthcare Limited

    K Number Device Name
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    K222528 Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode
    K220524 Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)
    K213091 Well-Life TENS/EMS/Heating Stimulator
    K200942 Well-Life Garment Electrodes (GM Series)
    K172809 OTC Combo TENS/EMS System
    K162663 WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605A
    K161453 WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A
    K141299 OTC COMBO TENS/EMS SYSTEM
    K133723 OTC PATCH
    Search all 22 clearances from Well-Life Healthcare Limited →