US HB2163 | 2017-2018 | 115th Congress
Status
Spectrum: Slight Partisan Bill (Democrat 2-1)
Status: Introduced on April 26 2017 - 25% progression, died in committee
Action: 2017-05-05 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Status: Introduced on April 26 2017 - 25% progression, died in committee
Action: 2017-05-05 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Summary
Medical Device Guardians Act This bill amends the Federal Food, Drug, and Cosmetic Act to require physicians to report significant adverse experiences caused by medical devices to the Food and Drug Administration.
Title
Medical Device Guardians Act
Sponsors
Rep. Brian Fitzpatrick [R-PA] | Rep. Louise Slaughter [D-NY] | Rep. Rosa DeLauro [D-CT] |
History
Date | Chamber | Action |
---|---|---|
2017-05-05 | House | Referred to the Subcommittee on Health. |
2017-04-26 | House | Referred to the House Committee on Energy and Commerce. |
2017-04-26 | House | Introduced in House |
Subjects
Drug safety, medical device, and laboratory regulation
Health
Health care quality
Health information and medical records
Health personnel
Health technology, devices, supplies
Product safety and quality
Health
Health care quality
Health information and medical records
Health personnel
Health technology, devices, supplies
Product safety and quality
US Congress State Sources
Type | Source |
---|---|
Summary | https://www.congress.gov/bill/115th-congress/house-bill/2163/all-info |
Text | https://www.congress.gov/115/bills/hr2163/BILLS-115hr2163ih.pdf |