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

    SURELOCK(TM) SNAPLESS MONITORING ELECTRODE

    K Number: K931903 · Decision Oct 7, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    5
    Review Days
    175

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    Basic Information

    Device Name
    SURELOCK(TM) SNAPLESS MONITORING ELECTRODE
    K Number
    K931903
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ludlow Technical Products
    Date Received
    April 15, 1993
    Decision Date
    October 7, 1993
    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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