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Preventing Superbugs and Protecting Patients Act
1/11/2023, 1:31 PM
Congressional Summary of S 2503
Preventing Superbugs and Protecting Patients Act
(Sec. 2) 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.
(Sec. 3) The FDA must issue final guidance regarding when a premarket notification is required for a modification to a medical device.Read the Full Bill
Current Status of Bill S 2503
Bill S 2503 is currently in the status of Bill Introduced since February 4, 2016. Bill S 2503 was introduced during Congress 114 and was introduced to the Senate on February 4, 2016. Bill S 2503's most recent activity was Placed on Senate Legislative Calendar under General Orders. Calendar No. 417. as of April 5, 2016
Bipartisan Support of Bill S 2503
Total Number of Sponsors
1Democrat Sponsors
1Republican Sponsors
0Unaffiliated Sponsors
0Total Number of Cosponsors
0Democrat Cosponsors
0Republican Cosponsors
0Unaffiliated Cosponsors
0Policy Area and Potential Impact of Bill S 2503
Primary Policy Focus
HealthPotential Impact Areas
- Administrative law and regulatory procedures
- Department of Health and Human Services
- Drug safety, medical device, and laboratory regulation
- Food and Drug Administration (FDA)
- Government information and archives
- Health technology, devices, supplies
- Infectious and parasitic diseases
Alternate Title(s) of Bill S 2503
Preventing Superbugs and Protecting Patients Act
A bill to establish requirements for reusable medical devices relating to cleaning instructions and validation data, and for other purposes.
Preventing Superbugs and Protecting Patients Act
Preventing Superbugs and Protecting Patients Act
Comments
Sponsors and Cosponsors of S 2503
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