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

    NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050

    K Number: K850477 · Decision Apr 29, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050
    K Number
    K850477
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Unisonic Products Corp.
    Date Received
    January 29, 1985
    Decision Date
    April 29, 1985
    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 Unisonic Products Corp.

    K Number Device Name
    K850476 NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-1050