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

    BLOOD PRESSURE UNIT MODEL 410

    K Number: K802412 · Decision Dec 16, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    420
    Registration Numbers
    420
    Same Product Code
    1186
    Applicant Total
    2
    Review Days
    74

    Basic Information

    Device Name
    BLOOD PRESSURE UNIT MODEL 410
    K Number
    K802412
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    JS & A GROUP
    Date Received
    October 3, 1980
    Decision Date
    December 16, 1980
    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 JS & A GROUP

    K Number Device Name
    K802411 BLOOD PRESSURE UNIT MODEL 310