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

    MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR

    K Number: K896102 · Decision Jan 18, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    14
    Review Days
    87

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    Basic Information

    Device Name
    MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR
    K Number
    K896102
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Advanced Medical Products, Inc.
    Date Received
    October 23, 1989
    Decision Date
    January 18, 1990
    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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