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

    MULTISCRIPTOR EK #403 VARIOUS MODEL

    K Number: K832014 · Decision Oct 31, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    177
    Registration Numbers
    177
    Same Product Code
    574
    Applicant Total
    38
    Review Days
    130

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    Basic Information

    Device Name
    MULTISCRIPTOR EK #403 VARIOUS MODEL
    K Number
    K832014
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Litton Medical Electronics
    Date Received
    June 23, 1983
    Decision Date
    October 31, 1983
    Product Code
    DPS
    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
    DPS Electrocardiograph

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