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510(k) Data Aggregation

    K Number
    K193070
    Device Name
    VIVACE Electrosurgical Device
    Manufacturer
    ShenB Co Ltd.
    Date Cleared
    2021-04-26

    (539 days)

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

    ShenB Co Ltd.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The VIVACE Electrosurgical System is intended for use in dermatologic and general surgical procedures for electrocoagulation and hemostasis and the percutaneous treatment of facial wrinkles for use with Fitzpatrick Skin Type I to Skin Type V when using the 1MHz setting. The 2MHz setting has not been evaluated for use in the percutaneous treatment of facial wrinkles and is intended for use in dermatologic and general surgical procedures for electrocoagulation and hemostasis.
    Device Description
    The VIVACE Electrosurgical System is comprised of the following components: - . The system main body, consisting of: - LCD touch screen control panel O - High-frequency generating output section (main P.C.B board or RF Generator) O - Power supply component Switch Mode Power Supply (SMPS) O - The accessories to the device include: ● - Handpiece with Handpiece Connector o - Disposable micro-needle cartridge (electrode) for insertion into Handpiece O - Foot switch O Radio frequency current (RF energy) is delivered from the RF Generator, through the handpiece and electrode tip into the target tissue. As RF energy passes through the skin, it generates an electro thermal reaction, which is capable of coagulating (causing minor dermal damage) the tissue. The bi-polar RF energy is delivered between independent adjacent electrode pairs (total 36 needle electrode, 6 x 6 array insertion). The RF generator and hand piece are not disposable micro-needle cartridge (electrode) is supplied sterile and is for single patient use only and cannot be re-sterilized.
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