BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

    LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70

    K Number: K023960 · Decision Jan 9, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    63
    Registration Numbers
    63
    Same Product Code
    176
    Applicant Total
    7
    Review Days
    41

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    Basic Information

    Device Name
    LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70
    K Number
    K023960
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1435
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Lidco, Ltd.
    Date Received
    November 29, 2002
    Decision Date
    January 9, 2003
    Product Code
    DXG
    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
    DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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