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

    ENOLOK-FOR ENDOSCOPED WITH 12.8>DIA.<13.3MM SHAFT DIAMETER, MODEL AEL; ENDOSCOPES WITH 11.3>DIA. 11.5MM SHAFT ,MODEL PEL

    K Number: K080317 · Decision Apr 29, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    111
    Applicant Total
    2
    Review Days
    83

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    ENOLOK-FOR ENDOSCOPED WITH 12.8>DIA.<13.3MM SHAFT DIAMETER, MODEL AEL; ENDOSCOPES WITH 11.3>DIA. 11.5MM SHAFT ,MODEL PEL
    K Number
    K080317
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Syntheon, LLC
    Date Received
    February 6, 2008
    Decision Date
    April 29, 2008
    Product Code
    FDF
    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
    FDF Colonoscope And Accessories, Flexible/Rigid

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (FDF), ordered by most recent decision date.

    Disposable Endoscopic Distal Attachments

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Disposable Distal End Tape Hood

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ROBOPERA (ER-R-002); ROBOPERA (ER-R-003)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FUJIFILM Endoscope Model EC-860P/M; FUJIFILM Endoscope Model EC-860P/L; FUJIFILM Endoscope Model EC-860S/L

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Colonovideoscope (CF-EZ1500DL); Colonovideoscope (CF-EZ1500DI); Gastrointestinal Videoscope (GIF-EZ1500)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PENTAX Medical Video Colonoscope (EC38-i20cWL)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology
    View all

    Other Clearances by Syntheon, LLC

    K Number Device Name
    K232295 LAA Exclusion System