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

    LumenR Tissue Retractor System

    K Number: K153698 · Decision Apr 19, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    118

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    Basic Information

    Device Name
    LumenR Tissue Retractor System
    K Number
    K153698
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Lumenr, LLC
    Date Received
    December 23, 2015
    Decision Date
    April 19, 2016
    Product Code
    ODB
    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
    ODB Endoscopic Contamination Prevention Sheath

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