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

    INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER

    K Number: K911840 · Decision Jun 3, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    47
    Registration Numbers
    47
    Same Product Code
    98
    Applicant Total
    17
    Review Days
    39

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    Basic Information

    Device Name
    INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER
    K Number
    K911840
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1240
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Intec Medical, Inc.
    Date Received
    April 25, 1991
    Decision Date
    June 3, 1991
    Product Code
    DYG
    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
    DYG Catheter, Flow Directed

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