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

    M VISUM ALERT ALARM MANAGEMENT SYSTEM

    K Number: K112282 · Decision Nov 4, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    72
    Registration Numbers
    72
    Same Product Code
    116
    Applicant Total
    1
    Review Days
    87

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    Basic Information

    Device Name
    M VISUM ALERT ALARM MANAGEMENT SYSTEM
    K Number
    K112282
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Mvisum, Inc.
    Date Received
    August 9, 2011
    Decision Date
    November 4, 2011
    Product Code
    MSX
    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
    MSX System, Network And Communication, Physiological Monitors

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