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

    KONTRON VITALMON 5010 PATIENT MONITOR

    K Number: K852249 · Decision Oct 16, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    109
    Registration Numbers
    109
    Same Product Code
    174
    Applicant Total
    57
    Review Days
    511

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    Basic Information

    Device Name
    KONTRON VITALMON 5010 PATIENT MONITOR
    K Number
    K852249
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.2375
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Kontron Instruments, Inc.
    Date Received
    May 23, 1985
    Decision Date
    October 16, 1986
    Product Code
    BZQ
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    BZQ Monitor, Breathing Frequency

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