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

    TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2

    K Number: K850655 · Decision Mar 7, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    130
    Applicant Total
    43
    Review Days
    16

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    Basic Information

    Device Name
    TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2
    K Number
    K850655
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Erika, Inc.
    Date Received
    February 19, 1985
    Decision Date
    March 7, 1985
    Product Code
    FJI
    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
    FJI Dialyzer, Capillary, Hollow Fiber

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    K852309 ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1
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