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.

The US Food and Drug Administration’s General Hospital and Personal Use Devices Panel of the Medical Devices Advisory Committee is set to meet 6 and 7 November in Gaithersburg, MD. A docket has been opened to collect comments before the meeting, the agency announced in a

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