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

    NOBLES-LAI IMAGING SYSTEM

    K Number: K920026 · Decision Jul 28, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    83
    Registration Numbers
    83
    Same Product Code
    97
    Applicant Total
    5
    Review Days
    207

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    Basic Information

    Device Name
    NOBLES-LAI IMAGING SYSTEM
    K Number
    K920026
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Nobles-Lai Engineering, Inc.
    Date Received
    January 3, 1992
    Decision Date
    July 28, 1992
    Product Code
    FET
    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
    FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology

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    Other Clearances by Nobles-Lai Engineering, Inc.

    K Number Device Name
    K953554 NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES
    K933345 NOBLES-LAI ENDOSCOPIC/LAPAROSCOPIC
    K914457 DISPOSABLE OPTICAL VALVULOTOME
    K895688 NOBLES-LAI ENGINEERING INFUSION PUMP