Health / Medical Topics

    Device Light Source Performance Evaluation Method

    Testing the optical properties of a device such as diopter, glare, and irradiance or glistening. (Food and Drug Administration)




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    Insufficient, inadequate, or incorrect information provided on a device's label or documentation regarding e.g. as the intended use, directions for use, and…
    Reviewing all labeling (including instructions for use, manuals, and packaging) for language related to reported device problems.
    Device problems that occur as the result of problems with the labeling (including package inserts, instruction manuals, instructions for use).
    Support contact information for a device labeler.
    An individual that labels a device.
    A device that is intended for one use, or on a single patient during a single procedure (Title 21 Chapter 9 Federal…

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