HR 2118
115th Congress
House
Health
Administrative law and regulatory procedures
Business records
Department of Health and Human Services
Drug safety, medical device, and laboratory regulation
Government information and archives
Health technology, devices, supplies
Licensing and registrations
Medical Device Servicing Safety and Accountability Act
Introduced: April 25, 2017
See on congress.gov
Everywhere this bill has been
3 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Apr 28, 2017
Referred to the Subcommittee on Health.
Apr 25, 2017
Referred to the House Committee on Energy and Commerce.
Apr 25, 2017
Introduced in House
Plain-English summary
Medical Device Servicing Safety and Accountability Act
This bill amends the Federal Food, Drug, and Cosmetic Act to require establishments servicing medical devices to register with the Food and Drug Administration (FDA). Such establishments must maintain records and make reports as the FDA requires to ensure the safety and effectiveness of serviced devices.
The bill exempts certain medical facilities, including physician's offices, that service medical devices in accordance with state and local laws.
What's happening now
Referred to the Subcommittee on Health.
Committees of jurisdiction
2