H.R. 4966 · 114th Congress

Preventing Superbugs and Protecting Patients Act

Stage
In committee
Sponsor
Ted Lieu
Introduced
2016-04-15
Latest action
2016-04-22 · Referred to the Subcommittee on Health.

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.