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

    BARD NEONATAL ECG MONITORING ELECTRODE

    K Number: K891075 · Decision Mar 22, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    645
    Review Days
    21

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    Basic Information

    Device Name
    BARD NEONATAL ECG MONITORING ELECTRODE
    K Number
    K891075
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    C.R. Bard, Inc.
    Date Received
    March 1, 1989
    Decision Date
    March 22, 1989
    Product Code
    DRX
    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
    DRX Electrode, Electrocardiograph

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