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

    ELECTROPHYSIOLOGY ELECTRODE CATH. W/SILVER/SILVER

    K Number: K881966 · Decision Oct 4, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    184
    Applicant Total
    645
    Review Days
    146

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    Basic Information

    Device Name
    ELECTROPHYSIOLOGY ELECTRODE CATH. W/SILVER/SILVER
    K Number
    K881966
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1220
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    C.R. Bard, Inc.
    Date Received
    May 11, 1988
    Decision Date
    October 4, 1988
    Product Code
    DRF
    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
    DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

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