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

    Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter

    K Number: K232505 · Decision May 30, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    6
    Review Days
    286

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    Basic Information

    Device Name
    Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter
    K Number
    K232505
    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
    Zhejiang Curaway Medical Technology Co., Ltd.
    Date Received
    August 18, 2023
    Decision Date
    May 30, 2024
    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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