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

    BREVET CASSETTE STERILIZATION MODULE

    K Number: K882617 · Decision Jul 28, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    875
    Registration Numbers
    875
    Same Product Code
    75
    Applicant Total
    6
    Review Days
    34

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    Basic Information

    Device Name
    BREVET CASSETTE STERILIZATION MODULE
    K Number
    K882617
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Brevet, Inc.
    Date Received
    June 24, 1988
    Decision Date
    July 28, 1988
    Product Code
    FSM
    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
    FSM Tray, Surgical, Instrument

    Similar 510(k) Clearances

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    SURGICAL INSTRUMENT TRAY

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    ARTHROSCOPY TRAY

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    OPEN HEART TRAY

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    HEART CATH TRAY

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