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

    S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0

    K Number: K002116 · Decision Aug 9, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    51
    Applicant Total
    14
    Review Days
    27

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    Basic Information

    Device Name
    S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0
    K Number
    K002116
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.4220
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medical Device Consultants, Inc.
    Date Received
    July 13, 2000
    Decision Date
    August 9, 2000
    Product Code
    DTQ
    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
    DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

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