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

    FLOORSTAND, FIBER OPTIC LIGHT SOURCE

    K Number: K760176 · Decision Aug 30, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59
    Same Product Code
    30
    Applicant Total
    41
    Review Days
    55

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    Basic Information

    Device Name
    FLOORSTAND, FIBER OPTIC LIGHT SOURCE
    K Number
    K760176
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    V. Mueller O.V. Baxter Healthcare Corp.
    Date Received
    July 6, 1976
    Decision Date
    August 30, 1976
    Product Code
    FCW
    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
    FCW Light Source, Fiberoptic, Routine

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