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

    REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCH

    K Number: K032632 · Decision Oct 22, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    104
    Registration Numbers
    104
    Same Product Code
    400
    Applicant Total
    7
    Review Days
    57

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    Basic Information

    Device Name
    REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCH
    K Number
    K032632
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    870.4210
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Estech, Inc.
    Date Received
    August 26, 2003
    Decision Date
    October 22, 2003
    Product Code
    DWF
    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
    DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

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