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

    BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES

    K Number: K911606 · Decision Jul 9, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    329
    Registration Numbers
    330
    Same Product Code
    61
    Applicant Total
    505
    Review Days
    90

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    Basic Information

    Device Name
    BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES
    K Number
    K911606
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Applicant
    Baxter Healthcare Corp
    Date Received
    April 10, 1991
    Decision Date
    July 9, 1991
    Product Code
    KDD
    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
    KDD Kit, Surgical Instrument, Disposable

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