FDA toughens rules on reusable medical devices
It issues new requirements on testing procedures in the wake of news that two people had died in California hospital from deadly bacteria traced to duodenoscopes
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Washington
THE US Food and Drug Administration said it is toughening testing procedures for manufacturers of reusable medical devices.
It issued the new requirements on Thursday in the wake of news that two people in a Los Angeles hospital had died from a deadly bacteria traced to medical scopes.
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