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

    Drive DeVilbiss iGo 2 Portable Oxygen Concentrator

    K Number: K172648 · Decision Mar 23, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    83
    Registration Numbers
    83
    Same Product Code
    286
    Applicant Total
    7
    Review Days
    203

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    Basic Information

    Device Name
    Drive DeVilbiss iGo 2 Portable Oxygen Concentrator
    K Number
    K172648
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5440
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Devilbiss Healthcare, LLC
    Date Received
    September 1, 2017
    Decision Date
    March 23, 2018
    Product Code
    CAW
    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
    CAW Generator, Oxygen, Portable

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