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

    MINIOX IA OXYGEN ANALYZER

    K Number: K935370 · Decision Aug 2, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    75
    Registration Numbers
    75
    Same Product Code
    273
    Applicant Total
    4
    Review Days
    271

    Basic Information

    Device Name
    MINIOX IA OXYGEN ANALYZER
    K Number
    K935370
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5440
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    MINE SAFETY APPLIANCES, CO.
    Date Received
    November 4, 1993
    Decision Date
    August 2, 1994
    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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