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

    HOME/COMMERCIAL OXYGEN UNIT BY SYSTEM O2

    K Number: K991569 · Decision Aug 3, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    83
    Registration Numbers
    83
    Same Product Code
    286
    Applicant Total
    1
    Review Days
    90

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    Basic Information

    Device Name
    HOME/COMMERCIAL OXYGEN UNIT BY SYSTEM O2
    K Number
    K991569
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5440
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    02 Marketing Group, Inc.
    Date Received
    May 5, 1999
    Decision Date
    August 3, 1999
    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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