H.R. 2915 · 116th Congress

Medical Device Guardians Act

Stage
In committee
Introduced
2019-05-22
Latest action
2019-05-23 · Referred to the Subcommittee on Health.

Summary

Medical Device Guardians Act

This bill requires physicians to report significant adverse experiences caused by medical devices to the Food and Drug Administration (FDA).

The FDA must establish an electronic reporting system to facilitate compliance with this bill and must publish the reports online.