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

    MICROLIFE AUTOMATIC TALKING BLOOD PRESSURE MONITOR

    K Number: K111652 · Decision Jul 13, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    54
    Review Days
    30

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    Basic Information

    Device Name
    MICROLIFE AUTOMATIC TALKING BLOOD PRESSURE MONITOR
    K Number
    K111652
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Microlife Intellectual Property GmbH
    Date Received
    June 13, 2011
    Decision Date
    July 13, 2011
    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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