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Device Sterilization, Duodenoscopes Focus Of Planned Meeting

 
• By Elizabeth Orr

The US FDA is asking stakeholders to weigh in on a common device sterilization procedure and the contagion risks of reprocessed duodenoscopes ahead of a November panel meeting.

FDA Advisory Committee Feature image

Stakeholders are being asked to weigh in on certain risks tied to device sterilization and reprocessed duodenoscopes as part of the lead-up to a November advisory panel meeting set to focus on those subjects.

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