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High-Risk Reprocessed SUD List Under Consideration By Device Center

This article was originally published in The Gray Sheet

Executive Summary

FDA may opt to create a list of reprocessed single-use devices (SUDs) that it considers to be "high" risk, Center for Devices and Radiological Health Office of Compliance Director Larry Spears reported at a Dec. 14 public meeting in Rockville, Maryland.

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FDA Single-Use Device Reuse Policy Expected To Solidify By Mid-2000

FDA's Center for Devices and Radiological Health plans to extend regulatory authority over reprocessing of single use devices (SUDs) by mid-2000.

High-Risk Reprocessed SUD List Under Consideration By Device Center

FDA may opt to create a list of reprocessed single-use devices (SUDs) that it considers to be "high" risk, Center for Devices and Radiological Health Office of Compliance Director Larry Spears reported at a Dec. 14 public meeting in Rockville, Maryland.

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