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

    DigitalDiagnost C50

    K Number: K201725 · Decision Jul 10, 2020
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    355
    Applicant Total
    1
    Review Days
    17

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    Basic Information

    Device Name
    DigitalDiagnost C50
    K Number
    K201725
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1680
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Philips Healthcare (Suzhou) Co., Lit.
    Date Received
    June 23, 2020
    Decision Date
    July 10, 2020
    Product Code
    KPR
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KPR System, X-Ray, Stationary

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