Fostering Innovation in Medical Imaging Act of 2017
Official title: To amend the Federal Food, Drug, and Cosmetic Act to provide clarity with respect to the regulation of diagnostic imaging devices intended for use with contrast agents.
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Referred to the Subcommittee on Health.
Fostering Innovation in Medical Imaging Act of 2017
This bill amends the Federal Food, Drug, and Cosmetic Act to allow the Food and Drug Administration (FDA) to approve a medical imaging device intended to be used with an approved contrast agent when—under specified conditions—the use differs from the approved use of the contrast agent. (Contrast agents are substances used to enhance the visibility of body structures in medical imaging.) The FDA center that reviews medical devices has primary jurisdiction over such reviews.
After authorization of a medical imaging device that makes new use of a contrast agent, the sponsor of the approved contrast agent may submit a supplemental application for the new use of the contrast agent.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 2009: Fostering Innovation in Medical Imaging Act of 2017. 115th Congress. Open America. https://openamerica.io/bill/115-HR-2009/
"H.R. 2009: Fostering Innovation in Medical Imaging Act of 2017." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-2009/.
H.R. 2009, 115th Cong. (2026), https://openamerica.io/bill/115-HR-2009/.
[H.R. 2009: Fostering Innovation in Medical Imaging Act of 2017](https://openamerica.io/bill/115-HR-2009/)