BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    MODELS M1175A AND M1176A COMPONENT MONITORING SYST

    K Number: K922058 · Decision Oct 6, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    121
    Registration Numbers
    121
    Same Product Code
    424
    Applicant Total
    230
    Review Days
    167

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    Basic Information

    Device Name
    MODELS M1175A AND M1176A COMPONENT MONITORING SYST
    K Number
    K922058
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1025
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Hewlett-Packard Co.
    Date Received
    April 22, 1992
    Decision Date
    October 6, 1992
    Product Code
    MHX
    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
    MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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