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

    Sinobot X1

    K Number: K220072 · Decision Jun 18, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    250
    Registration Numbers
    250
    Same Product Code
    422
    Applicant Total
    1
    Review Days
    524

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    Basic Information

    Device Name
    Sinobot X1
    K Number
    K220072
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.4560
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sinovation (Beijing) Medical Technology Co., Ltd.
    Date Received
    January 10, 2022
    Decision Date
    June 18, 2023
    Product Code
    HAW
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HAW Neurological Stereotaxic Instrument

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