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

    ACCUCOM CARDIAC OUTPUT MONITOR

    K Number: K851426 · Decision Jul 12, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    77
    Applicant Total
    4
    Review Days
    93

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    Basic Information

    Device Name
    ACCUCOM CARDIAC OUTPUT MONITOR
    K Number
    K851426
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Lawrence Medical Systems, Inc.
    Date Received
    April 10, 1985
    Decision Date
    July 12, 1985
    Product Code
    DXK
    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
    DXK Echocardiograph

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    Other Clearances by Lawrence Medical Systems, Inc.

    K Number Device Name
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    K862548 TEMPERATURE SENSING ESOPHAGEAL TRANSDUCER