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

    PEI PLAQUE ELECTRODE ARRAY

    K Number: K904747 · Decision Oct 9, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    184
    Applicant Total
    6
    Review Days
    355

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    Basic Information

    Device Name
    PEI PLAQUE ELECTRODE ARRAY
    K Number
    K904747
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1220
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Prucka Engineering, Inc.
    Date Received
    October 19, 1990
    Decision Date
    October 9, 1991
    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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