S 3395 United States Senate · 117th Congress

Medical Device Integrity Act

Summary
Medical Device Integrity Act This bill provides the Food and Drug Administration (FDA) with the authority to request records and information from an establishment that manufactures or otherwise prepares medical devices. Currently, the FDA only has statutory authority to make such requests to establishments that manufacture or otherwise prepare drugs. The bill also requires the FDA to include in its requests a rationale for requesting the information in question.
Bill status in committee 1 of 4 stages cleared
Introduction
Dec 2021
Committee Review
Floor Vote
President
Introduced Dec 14, 2021 Last action Dec 14, 2021
Floor votes

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Full legislative history

Actions timeline

Total actions
2
Key actions
0
Committee
1
Dec 14, 2021
Committee
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
upper
Dec 14, 2021
Introduced
Introduced in Senate
upper
1 primary · 2 co-sponsors

Sponsors