BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

    NR5000 E.C.G. AND PULSE OXIMETER MONITOR

    K Number: K894919 · Decision Sep 18, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    103
    Registration Numbers
    103
    Same Product Code
    338
    Applicant Total
    2
    Review Days
    47

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    Basic Information

    Device Name
    NR5000 E.C.G. AND PULSE OXIMETER MONITOR
    K Number
    K894919
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Nirad , Ltd.
    Date Received
    August 2, 1989
    Decision Date
    September 18, 1989
    Product Code
    DRT
    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
    DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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