BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    STUART LEE CLIP

    K Number: K881741 · Decision Jun 3, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    270
    Registration Numbers
    270
    Same Product Code
    31
    Applicant Total
    1
    Review Days
    42

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    Basic Information

    Device Name
    STUART LEE CLIP
    K Number
    K881741
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Stuart-Lee, Inc.
    Date Received
    April 22, 1988
    Decision Date
    June 3, 1988
    Product Code
    GDJ
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GDJ Clamp, Surgical, General & Plastic Surgery

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