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

    ECC.O SYSTEM

    K Number: K050890 · Decision May 5, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35
    Same Product Code
    83
    Applicant Total
    6
    Review Days
    27

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    Basic Information

    Device Name
    ECC.O SYSTEM
    K Number
    K050890
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.4360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Dideco S.R.L.
    Date Received
    April 8, 2005
    Decision Date
    May 5, 2005
    Product Code
    KFM
    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
    KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

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