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

    DEVILBISS MODEL 1400D (OXYGEN CONSERVING DEVICE)

    K Number: K890141 · Decision Apr 6, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    15
    Registration Numbers
    15
    Same Product Code
    69
    Applicant Total
    29
    Review Days
    83

    Basic Information

    Device Name
    DEVILBISS MODEL 1400D (OXYGEN CONSERVING DEVICE)
    K Number
    K890141
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5905
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    DEVILBISS HEALTH CARE, INC.
    Date Received
    January 13, 1989
    Decision Date
    April 6, 1989
    Product Code
    NFB
    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
    NFB Conserver, Oxygen

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