FDA orders duodenoscope manufacturers to conduct postmarket surveillance studies in health care facilities

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Title: FDA orders duodenoscope manufacturers to conduct postmarket surveillance studies in health care facilities

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10/05/2015 11:09 AM EDT

The U.S. Food and Drug Administration today ordered the three manufacturers of duodenoscopes marketed in the U.S. to conduct postmarket surveillance studies to better understand how the devices are reprocessed in real-world settings.

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