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    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Victan

    K Number: K230593 · Decision May 30, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    2
    Review Days
    88

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    Basic Information

    Device Name
    Victan
    K Number
    K230593
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Jiangsu Haize Medical Scientific Development Co., Ltd.
    Date Received
    March 3, 2023
    Decision Date
    May 30, 2023
    Product Code
    GEI
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GEI Electrosurgical, Cutting & Coagulation & Accessories

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