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

    PRIMARY SURGICAL DRESSING TRAY

    K Number: K922041 · Decision Nov 6, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    21
    Review Days
    189

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    Basic Information

    Device Name
    PRIMARY SURGICAL DRESSING TRAY
    K Number
    K922041
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Transidyne General Corp.
    Date Received
    May 1, 1992
    Decision Date
    November 6, 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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