Providing for congressional disapproval under chapter 8 of title 5, United States Code, of the rule submitted by the Food and Drug Administration relating to "Medical Devices; Laboratory Developed Tests".

[Congressional Bills 118th Congress] [From the U.S. Government Publishing Office] [H.J. Res. 145 Introduced in House (IH)]

118th CONGRESS 2d Session H. J. RES. 145

Providing for congressional disapproval under chapter 8 of title 5, United States Code, of the rule submitted by the Food and Drug Administration relating to "Medical Devices; Laboratory Developed Tests".

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IN THE HOUSE OF REPRESENTATIVES

May 16, 2024

Mr. Finstad (for himself and Mr. Crenshaw) submitted the following joint resolution; which was referred to the Committee on Energy and Commerce

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JOINT RESOLUTION

Providing for congressional disapproval under chapter 8 of title 5, United States Code, of the rule submitted by the Food and Drug Administration relating to "Medical Devices; Laboratory Developed Tests".

Resolved by the Senate and House of Representatives of the United States of America in Congress assembled, That Congress disapproves the rule submitted by the Food and Drug Administration relating to "Medical Devices; Laboratory Developed Tests" (89 Fed. Reg. 37286; May 6, 2024), and such rule shall have no force or effect.