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

    BUTTON LUBRICATOR

    K Number: K951713 · Decision Apr 25, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    5
    Applicant Total
    2
    Review Days
    11

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    Basic Information

    Device Name
    BUTTON LUBRICATOR
    K Number
    K951713
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Fibertech Instruments, Inc.
    Date Received
    April 14, 1995
    Decision Date
    April 25, 1995
    Product Code
    FHX
    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
    FHX Jelly, Lubricating, For Transurethral Surgical Instrument

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