skip to main content

H.R. 2118 (115th): Medical Device Servicing Safety and Accountability Act

We don’t have a summary available yet.

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress, and was published on Apr 25, 2017.


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.