BEUDAMED
    FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

    ACCUFIX AND LASERDISH BIPOLAR VS-1 LEADS

    K Number: K884811 · Decision Feb 22, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24
    Same Product Code
    486
    Applicant Total
    1
    Review Days
    97

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    Basic Information

    Device Name
    ACCUFIX AND LASERDISH BIPOLAR VS-1 LEADS
    K Number
    K884811
    Device Class
    FDA class 3
    Clearance Type
    Traditional
    Regulation Number
    870.3680
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Telectronics and Control Pacing Systems
    Date Received
    November 17, 1988
    Decision Date
    February 22, 1989
    Product Code
    DTB
    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
    DTB Permanent Pacemaker Electrode

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