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

    ECG ELECTRODE SYSTEM

    K Number: K873442 · Decision Nov 23, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    1
    Review Days
    88

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    Basic Information

    Device Name
    ECG ELECTRODE SYSTEM
    K Number
    K873442
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S
    Date Received
    August 27, 1987
    Decision Date
    November 23, 1987
    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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