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

    Fiber Laser Treatment System

    K Number: K221770 · Decision Oct 13, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    57
    Registration Numbers
    57
    Same Product Code
    34
    Applicant Total
    14
    Review Days
    114

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    Basic Information

    Device Name
    Fiber Laser Treatment System
    K Number
    K221770
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Shanghai Apolo Medical Technology Co., Ltd.
    Date Received
    June 21, 2022
    Decision Date
    October 13, 2022
    Product Code
    ONG
    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
    ONG Powered Laser Surgical Instrument With MicrobeamFractional Output

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    Other Clearances by Shanghai Apolo Medical Technology Co., Ltd.

    K Number Device Name
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