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

    ETHICON TEMPORARY CARDIAC PACING WIRE

    K Number: K822155 · Decision Aug 24, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    128
    Applicant Total
    204
    Review Days
    32

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    Basic Information

    Device Name
    ETHICON TEMPORARY CARDIAC PACING WIRE
    K Number
    K822155
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.3680
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    ETHICON, Inc.
    Date Received
    July 23, 1982
    Decision Date
    August 24, 1982
    Product Code
    LDF
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LDF Electrode, Pacemaker, Temporary

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