BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    KLOCK WATCH STYLE DIGITAL BLOOD PRESSURE MONITOR

    K Number: K023356 · Decision Jan 16, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    172
    Registration Numbers
    172
    Same Product Code
    197
    Applicant Total
    49
    Review Days
    101

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    Basic Information

    Device Name
    KLOCK WATCH STYLE DIGITAL BLOOD PRESSURE MONITOR
    K Number
    K023356
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1120
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Card Guard Scientific Survival , Ltd.
    Date Received
    October 7, 2002
    Decision Date
    January 16, 2003
    Product Code
    DXQ
    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
    DXQ Blood Pressure Cuff

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    Other Clearances by Card Guard Scientific Survival , Ltd.

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