BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822

    K Number: K014204 · Decision Mar 5, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    26
    Review Days
    74

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    Basic Information

    Device Name
    ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822
    K Number
    K014204
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    K-Jump Health Co., Ltd.
    Date Received
    December 21, 2001
    Decision Date
    March 5, 2002
    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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