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510(k) Data Aggregation

    K Number
    K213814
    Device Name
    Viveve 2.0 System
    Manufacturer
    Date Cleared
    2022-02-02

    (57 days)

    Product Code
    Regulation Number
    878.4400
    Why did this record match?
    Applicant Name (Manufacturer) :

    Viveve, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The Viveve 2.0 System is indicated for use in general surgical procedures for electrocoagulation and hemostasis.
    Device Description
    The Viveve 2.0 System utilizes monopolar radiofrequency (RF) energy to selectively heat a given volume of tissue beneath the surface, while cryogen is delivered to the inside of the treatment tip to cool the surface tissue. The generator delivers energy to the treatment tip to create an electric field under the treatment tip (electrode). The mechanism of action is the application of RF energy to the tissue causing coagulation and/or hemostasis. The Viveve® 2.0 System consists of four (4) primary components: - . An RF Generator to provide the heating energy. The Generator incorporates the Cooling Module to supply coolant which provides the cooling energy. - . A hand piece that couples the cooling and heating energy to the tissue through the treatment tip. - A footswitch that allows the user to turn the RF Energy on or off. - 5cm or 8cm Sterile Disposable Treatment Tips. Accessories include: - . Coupling Fluid - Cryogen ● - Return Cable ● - Return Pad ● - . Power Cord
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