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

    SR-1000 Portable DR Imaging System, SR-1000S Portable DR Imaging System

    K Number: K202350 · Decision Jan 6, 2021
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    235
    Applicant Total
    8
    Review Days
    141

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    Basic Information

    Device Name
    SR-1000 Portable DR Imaging System, SR-1000S Portable DR Imaging System
    K Number
    K202350
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1720
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui)
    Date Received
    August 18, 2020
    Decision Date
    January 6, 2021
    Product Code
    IZL
    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
    IZL System, X-Ray, Mobile

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