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

    ORTHOPEDIC TRAY PRODUCT LINE

    K Number: K940646 · Decision Mar 11, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    285
    Registration Numbers
    286
    Same Product Code
    21
    Applicant Total
    1
    Review Days
    24

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    Basic Information

    Device Name
    ORTHOPEDIC TRAY PRODUCT LINE
    K Number
    K940646
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Cushindu
    Date Received
    February 15, 1994
    Decision Date
    March 11, 1994
    Product Code
    LRP
    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
    LRP Tray, Surgical

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