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

    SUITCASE KIDNEY HEMODIALYSIS SYSTEM

    K Number: K781405 · Decision Dec 7, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    49
    Applicant Total
    69
    Review Days
    115

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    Basic Information

    Device Name
    SUITCASE KIDNEY HEMODIALYSIS SYSTEM
    K Number
    K781405
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Union Carbide Corp.
    Date Received
    August 14, 1978
    Decision Date
    December 7, 1978
    Product Code
    FKP
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FKP System, Dialysate Delivery, Single Patient

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