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

    I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)

    K Number: K760263 · Decision Aug 4, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    14
    Applicant Total
    2
    Review Days
    14

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    Basic Information

    Device Name
    I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)
    K Number
    K760263
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5955
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Foregger
    Date Received
    July 21, 1976
    Decision Date
    August 4, 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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