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

    3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE

    K Number: K934333 · Decision Jul 7, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    12
    Review Days
    303

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    Basic Information

    Device Name
    3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE
    K Number
    K934333
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    3M Medical Products Group
    Date Received
    September 7, 1993
    Decision Date
    July 7, 1994
    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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