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

    WRIST AUTOMATIC BLOOD PRESSURE MONITOR

    K Number: K131463 · Decision Jul 8, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    12
    Review Days
    48

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    Basic Information

    Device Name
    WRIST AUTOMATIC BLOOD PRESSURE MONITOR
    K Number
    K131463
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Honsun (Nantong) Co., Ltd.
    Date Received
    May 21, 2013
    Decision Date
    July 8, 2013
    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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