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

    NASAL AIRE II PEDIATRIC, MODEL 5 SIZES, MODEL TBD

    K Number: K090804 · Decision Nov 5, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    118
    Registration Numbers
    118
    Same Product Code
    459
    Applicant Total
    2
    Review Days
    225

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    Basic Information

    Device Name
    NASAL AIRE II PEDIATRIC, MODEL 5 SIZES, MODEL TBD
    K Number
    K090804
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5905
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Innomed Technologies, Inc./Respcare, Inc.
    Date Received
    March 25, 2009
    Decision Date
    November 5, 2009
    Product Code
    BZD
    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
    BZD Ventilator, Non-Continuous (Respirator)

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    Other Clearances by Innomed Technologies, Inc./Respcare, Inc.

    K Number Device Name
    K062019 RESPCARE HYBRID NE FACE MASK, MODEL TBD,; DISPOSABLE, MODEL TBD