To prohibit the use of Federal funds to implement, administer, or enforce a final rule of the Food and Drug Administration relating to "Medical Devices; Laboratory Developed Tests", and for other purposes.
This bill seeks to prevent the implementation, administration, or enforcement of a specific Food and Drug Administration (FDA) final rule by prohibiting the use of Federal funds for these activities. The targeted rule, titled "Medical Devices; Laboratory Developed Tests," was submitted for publication in the Federal Register on May 6, 2024, and identified as 89 Fed. Reg. 37286. The legislation explicitly states that no Federal funds may be used for any aspect of this rule, or for any regulation deemed substantially similar to it. This measure effectively aims to halt the progression and application of the FDA's regulatory framework concerning laboratory developed tests.
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Timeline
Introduced in House
Referred to the House Committee on Energy and Commerce.
Introduced in House
Referred to the House Committee on Energy and Commerce.
Health
Administrative law and regulatory proceduresDrug safety, medical device, and laboratory regulationFood and Drug Administration (FDA)Health programs administration and fundingMedical tests and diagnostic methods
To prohibit the use of Federal funds to implement, administer, or enforce a final rule of the Food and Drug Administration relating to "Medical Devices; Laboratory Developed Tests", and for other purposes.
USA119th CongressHR-1463| House
| Updated: 2/21/2025
This bill seeks to prevent the implementation, administration, or enforcement of a specific Food and Drug Administration (FDA) final rule by prohibiting the use of Federal funds for these activities. The targeted rule, titled "Medical Devices; Laboratory Developed Tests," was submitted for publication in the Federal Register on May 6, 2024, and identified as 89 Fed. Reg. 37286. The legislation explicitly states that no Federal funds may be used for any aspect of this rule, or for any regulation deemed substantially similar to it. This measure effectively aims to halt the progression and application of the FDA's regulatory framework concerning laboratory developed tests.
Administrative law and regulatory proceduresDrug safety, medical device, and laboratory regulationFood and Drug Administration (FDA)Health programs administration and fundingMedical tests and diagnostic methods