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

    LAPAROSCOPIC VESSEL ARTICULATOR

    K Number: K911475 · Decision Jul 2, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    45
    Registration Numbers
    45
    Same Product Code
    19
    Applicant Total
    94
    Review Days
    89

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    Basic Information

    Device Name
    LAPAROSCOPIC VESSEL ARTICULATOR
    K Number
    K911475
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4475
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    United States Endoscopy Group, Inc.
    Date Received
    April 4, 1991
    Decision Date
    July 2, 1991
    Product Code
    DWP
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DWP Dilator, Vessel, Surgical

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