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510(k) Data Aggregation

    K Number
    K161484
    Device Name
    ZIIP Device
    Manufacturer
    ZIIP,LLC
    Date Cleared
    2017-02-24

    (269 days)

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

    ZIIP,LLC

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The ZIIP Device is intended for facial 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. It is intended to be used by a single user (multiple applications).
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