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United States · Bill · HR

H.R. 88 (119th)

Medical Innovation Acceleration Act of 2025

referredUnited States· United States Congress· EN

Introduced

3 January 2025

Last action

—

Status

Referred to the House Committee on Energy and Commerce.

Sponsors

—

Subjects

Discovery layer

Source updated

14 January 2026

Summary

Medical Innovation Acceleration Act of 2025 This bill exempts noninvasive diagnostic devices from the regulatory authority of the Food and Drug Administration. 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.

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Documents

2 official files

Introduced in House

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Sources

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