Preventing Superbugs and Protecting Patients Act

Summary

Preventing Superbugs and Protecting Patients Act This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to identify types of medical devices for which premarket notification must include proposed labeling, including validated instructions regarding cleaning, disinfection, and sterilization. The FDA must issue final guidance regarding when a premarket notification is required for a modification to a medical device.

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3 official files

• Introduced in House (text)

  Introduced in House · EN · 15 April 2016

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• Introduced in House (PDF)

  Introduced in House · EN · 15 April 2016

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• Introduced in House

  summary · EN · 15 April 2016

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