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510(k) Data Aggregation

    K Number
    K212342
    Device Name
    ZIIP+ Device
    Manufacturer
    ZIIP, Inc
    Date Cleared
    2021-09-23

    (57 days)

    Product Code
    NFO
    Regulation Number
    882.5890
    Why did this record match?
    Applicant Name (Manufacturer) :

    ZIIP, Inc

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The ZIIP+ Device is indicated for facial and neck stimulation and is indicated for over-the-counter cosmetic use.
    Device Description
    The ZIIP+ Device is a hand-held, battery-powered device used with conductive gel to stimulate the face superficially through application of transcutaneous electrical currents. The device is powered by a Lithium-lon rechargeable battery, and it is shipped with a portable battery charger.
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