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

    ARGYLE DUAL STAGE VENOUS RETURN CATH.

    K Number: K831332 · Decision Jun 30, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    104
    Registration Numbers
    104
    Same Product Code
    400
    Applicant Total
    191
    Review Days
    66

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    Basic Information

    Device Name
    ARGYLE DUAL STAGE VENOUS RETURN CATH.
    K Number
    K831332
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4210
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Sherwood Medical Co.
    Date Received
    April 25, 1983
    Decision Date
    June 30, 1983
    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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