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

    PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO

    K Number: K954980 · Decision May 15, 1996
    View on FDA
    Classifications
    0
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    82
    Applicant Total
    230
    Review Days
    197

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    Basic Information

    Device Name
    PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO
    K Number
    K954980
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Hewlett-Packard Co.
    Date Received
    October 31, 1995
    Decision Date
    May 15, 1996
    Product Code
    LOS
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

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