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

    LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER

    K Number: K922190 · Decision Oct 23, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    21
    Review Days
    165

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    Basic Information

    Device Name
    LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
    K Number
    K922190
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Advanced Surgical, Inc.
    Date Received
    May 11, 1992
    Decision Date
    October 23, 1992
    Product Code
    FMF
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FMF Syringe, Piston

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