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

    BRIOX MODEL-AEROMIST

    K Number: K800078 · Decision Feb 5, 1980
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    6
    Review Days
    22

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    Basic Information

    Device Name
    BRIOX MODEL-AEROMIST
    K Number
    K800078
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Briox Technologies, Inc.
    Date Received
    January 14, 1980
    Decision Date
    February 5, 1980
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

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    K791238 BRIOX MODEL 2000-CQ QUIET COMPRESSOR
    K791240 BRIOX MODEL 2000-C COMPRESSOR UNIT
    K791241 BRIOX MODEL 2000-CA COMPRESSOR UNIT
    K791239 BRIOX MODEL 2000-A ASPIRATOR UNIT