There is 1 version of this bill. View text

Click the check-box to add or remove the section, click the text link to scroll to that section.
Titles Actions Overview All Actions Cosponsors Committees Related Bills Subjects Latest Summary All Summaries

Titles (2)

Short Titles

Short Titles - House of Representatives

Short Titles as Introduced

Medical Device Guardians Act of 2016

Official Titles

Official Titles - House of Representatives

Official Title as Introduced

To amend the Federal Food, Drug, and Cosmetic Act to require physicians and physician's offices to be treated as covered device users required to report on certain adverse events involving medical devices, and for other purposes.


Actions Overview (1)

Date
06/08/2016 Introduced in House

All Actions (2)

Date
06/08/2016 Referred to the House Committee on Energy and Commerce.
Action By: House of Representatives
06/08/2016 Introduced in House
Action By: House of Representatives

Committees (1)

Committees, subcommittees and links to reports associated with this bill are listed here, as well as the nature and date of committee activity and Congressional report number.

Committee / Subcommittee Date Activity Reports
House Energy and Commerce06/08/2016 Referred to

Related Bills (0)

No related bill information was received for H.R.5404.

Subjects (7)

  • Drug safety, medical device, and laboratory regulation
  • Health care quality
  • Health information and medical records
  • Health personnel
  • Health technology, devices, supplies
  • Product safety and quality

Latest Summary (1)

There is one summary for H.R.5404. View summaries

Shown Here:
Introduced in House (06/08/2016)

Medical Device Guardians Act of 2016

This bill amends the Federal Food, Drug, and Cosmetic Act by requiring physicians to report to the Food and Drug Administration about significant adverse experiences caused by medical devices.