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

    Digital Thermometer

    K Number: K230889 · Decision Apr 3, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    3
    Review Days
    369

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    Basic Information

    Device Name
    Digital Thermometer
    K Number
    K230889
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Wenzhou Yosun Medical Technology Co.,Ltd
    Date Received
    March 31, 2023
    Decision Date
    April 3, 2024
    Product Code
    FLL
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FLL Continuous Measurement Thermometer

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    Other Clearances by Wenzhou Yosun Medical Technology Co.,Ltd

    K Number Device Name
    K231478 Digital Blood Pressure Monitor (Model: YB-800)
    K201843 Infrared ear and forehead thermometer, model YI-100