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

    BRIOX MODEL 2000-CA COMPRESSOR UNIT

    K Number: K791241 · Decision Jul 24, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    64
    Registration Numbers
    64
    Same Product Code
    76
    Applicant Total
    6
    Review Days
    18

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    Basic Information

    Device Name
    BRIOX MODEL 2000-CA COMPRESSOR UNIT
    K Number
    K791241
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4780
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Briox Technologies, Inc.
    Date Received
    July 6, 1979
    Decision Date
    July 24, 1979
    Product Code
    JCX
    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
    JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

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    Other Clearances by Briox Technologies, Inc.

    K Number Device Name
    K813507 INFALERT
    K800078 BRIOX MODEL-AEROMIST
    K791238 BRIOX MODEL 2000-CQ QUIET COMPRESSOR
    K791240 BRIOX MODEL 2000-C COMPRESSOR UNIT
    K791239 BRIOX MODEL 2000-A ASPIRATOR UNIT