HR. 88In Committee
Medical Innovation Acceleration Act of 2025
Exempts qualifying noninvasive diagnostic devices from Food and Drug Administration regulation and defines which devices meet that standard
Plain-English overview
What this bill does
Exempts qualifying noninvasive diagnostic devices from Food and Drug Administration regulation and defines which devices meet that standard
Key points
- Establish device qualification standard
- Exempt noninvasive diagnostic devices
Current status
Where it stands
Status
In Committee
Latest action
2025-01-03 — Referred to the House Committee on Energy and Commerce.
Related context
Topics and policy areas
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