H.R. 2118 · 115th Congress

Medical Device Servicing Safety and Accountability Act

Stage
In committee
Introduced
2017-04-25
Latest action
2017-04-28 · Referred to the Subcommittee on Health.

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.