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

    INSPIRON I.M.V. SET UP

    K Number: K760891 · Decision Dec 9, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    14
    Applicant Total
    20
    Review Days
    44

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    Basic Information

    Device Name
    INSPIRON I.M.V. SET UP
    K Number
    K760891
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5955
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Inspiron Corp.
    Date Received
    October 26, 1976
    Decision Date
    December 9, 1976
    Product Code
    CBO
    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
    CBO Attachment, Intermittent Mandatory Ventilation (Imv)

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