United StatesMedical Innovation Acceleration Act of 2025
What it does
This bill exempts noninvasive diagnostic devices from the regulatory authority of the Food and Drug Administration.
More detail
The bill defines noninvasive diagnostic device as one that does not penetrate the skin or any other membrane of the body, is not inserted or implanted into the body, causes no more than ephemeral compression or temperature changes to in situ bodily tissues, and does not subject bodily tissues to ionizing radiation.
Where do you stand?
Choose your position
Tell your reps
Take a position to see your representatives and ways to contact them.
Where it stands
- Introduced
- Passed House
- Passed Senate
- To President
- Became Law
Looking ahead
No hearings or votes scheduled.
History
- 2025
- Jan 3Introduced in HouseLatest
- Jan 3Referred to the House Committee on Energy and Commerce.Introduced