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

    RHINOMANOMETER

    K Number: K896263 · Decision Apr 16, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    11
    Applicant Total
    92
    Review Days
    167

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    Basic Information

    Device Name
    RHINOMANOMETER
    K Number
    K896263
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1800
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Jedmed Instrument Co.
    Date Received
    October 31, 1989
    Decision Date
    April 16, 1990
    Product Code
    BXQ
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    BXQ Rhinoanemometer (Measurement Of Nasal Decongestion)

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