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

    MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE

    K Number: K862251 · Decision Sep 4, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    127
    Registration Numbers
    127
    Same Product Code
    205
    Applicant Total
    2
    Review Days
    84

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    Basic Information

    Device Name
    MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE
    K Number
    K862251
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5250
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Bio-Flow, Inc.
    Date Received
    June 12, 1986
    Decision Date
    September 4, 1986
    Product Code
    KNX
    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
    KNX Collector, Urine, (And Accessories) For Indwelling Catheter

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    Other Clearances by Bio-Flow, Inc.

    K Number Device Name
    K851266 QRI-FLOW URINE FLOW MEASURING DEVICE