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

    Arm Blood Pressure Monitor

    K Number: K192023 · Decision Dec 23, 2019
    View on FDA
    Classifications
    1
    FEI Numbers
    420
    Registration Numbers
    420
    Same Product Code
    1186
    Applicant Total
    2
    Review Days
    147

    Basic Information

    Device Name
    Arm Blood Pressure Monitor
    K Number
    K192023
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Truly Instrument Limited
    Date Received
    July 29, 2019
    Decision Date
    December 23, 2019
    Product Code
    DXN
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXN System, Measurement, Blood-Pressure, Non-Invasive

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    Other Clearances by Truly Instrument Limited

    K Number Device Name
    K220276 Infrared Thermometer TET-351