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

    CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY

    K Number: K912158 · Decision Oct 23, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    205
    Same Product Code
    503
    Applicant Total
    30
    Review Days
    160

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    Basic Information

    Device Name
    CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY
    K Number
    K912158
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Medical Device Inspection Co., Inc.
    Date Received
    May 16, 1991
    Decision Date
    October 23, 1991
    Product Code
    FOZ
    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
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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