BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    MEDITECH AMBULATORY BLOOD PRESSURE MONITOR, MODEL ABPM-05

    K Number: K071960 · Decision Aug 3, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    2
    Review Days
    18

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    Basic Information

    Device Name
    MEDITECH AMBULATORY BLOOD PRESSURE MONITOR, MODEL ABPM-05
    K Number
    K071960
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Meditech Kft.
    Date Received
    July 16, 2007
    Decision Date
    August 3, 2007
    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 Meditech Kft.

    K Number Device Name
    K051149 MEDITECH MODEL ABPM-04