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

    RSI FEMORAL GUIDING CATHETER

    K Number: K902943 · Decision Oct 3, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    210
    Registration Numbers
    211
    Same Product Code
    499
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    RSI FEMORAL GUIDING CATHETER
    K Number
    K902943
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Retroperfusion Systems, Inc.
    Date Received
    July 5, 1990
    Decision Date
    October 3, 1990
    Product Code
    DQO
    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
    DQO Catheter, Intravascular, Diagnostic

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    Other Clearances by Retroperfusion Systems, Inc.

    K Number Device Name
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