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

    ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2

    K Number: K121724 · Decision Sep 20, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59
    Same Product Code
    30
    Applicant Total
    142
    Review Days
    100

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    Basic Information

    Device Name
    ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2
    K Number
    K121724
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Richard Wolf Medical Instruments Corp.
    Date Received
    June 12, 2012
    Decision Date
    September 20, 2012
    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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