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

    JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS

    K Number: K020784 · Decision Jan 9, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    104
    Registration Numbers
    104
    Same Product Code
    400
    Applicant Total
    13
    Review Days
    304

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    Basic Information

    Device Name
    JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS
    K Number
    K020784
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4210
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Jostra AG
    Date Received
    March 11, 2002
    Decision Date
    January 9, 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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