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

    IBM 5885 DIGITAL ECG ACQUISITION CART

    K Number: K810988 · Decision May 1, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    177
    Registration Numbers
    177
    Same Product Code
    574
    Applicant Total
    8
    Review Days
    18

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    Basic Information

    Device Name
    IBM 5885 DIGITAL ECG ACQUISITION CART
    K Number
    K810988
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Intl. Business Machines
    Date Received
    April 13, 1981
    Decision Date
    May 1, 1981
    Product Code
    DPS
    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
    DPS Electrocardiograph

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    Other Clearances by Intl. Business Machines

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    K771258 BLOOD CELL SEPARATOR 2997
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