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

    FLOW-DIRECTED THERMODILUTION CATH

    K Number: K843409 · Decision Oct 18, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    47
    Registration Numbers
    47
    Same Product Code
    98
    Applicant Total
    21
    Review Days
    48

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    Basic Information

    Device Name
    FLOW-DIRECTED THERMODILUTION CATH
    K Number
    K843409
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1240
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Andover Medical, Inc.
    Date Received
    August 31, 1984
    Decision Date
    October 18, 1984
    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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    K860535 UNILATERAL OXYGEN DELIVERY SYSTEM (ULODS)
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