BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    NEPHROSS 11F100

    K Number: K790352 · Decision Feb 22, 1979
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    —

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    Basic Information

    Device Name
    NEPHROSS 11F100
    K Number
    K790352
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    Redy Laboratories
    Date Received
    February 22, 1979
    Decision Date
    February 22, 1979
    Advisory Committee
    Unknown
    Review Advisory Committee
    GU
    Third Party
    N

    Other Clearances by Redy Laboratories

    K Number Device Name
    K772290 DIALYZER, CAPILATORY, HOLLOW FIBER