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

    DIALYZER, CAPILATORY, HOLLOW FIBER

    K Number: K772290 · Decision Mar 15, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    130
    Applicant Total
    2
    Review Days
    93

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    Basic Information

    Device Name
    DIALYZER, CAPILATORY, HOLLOW FIBER
    K Number
    K772290
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Redy Laboratories
    Date Received
    December 12, 1977
    Decision Date
    March 15, 1978
    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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