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United States · Bill · HR

H.R. 2058 (114th)

FDA Deeming Authority Clarification Act of 2015

referredUnited States· United States Congress· EN

Introduced

28 April 2015

Last action

1 May 2015 · Referred

Status

Referred to the Subcommittee on Health.

Sponsors

Rep. Cole, Tom [R-OK-4], Rep. Rouzer, David [R-NC-7], Rep. Guthrie, Brett [R-KY-2], Rep. Rooney, Thomas J. [R-FL-17], Rep. Hunter, Duncan D. [R-CA-50], Rep. Amodei, Mark E. [R-NV-2], Rep. Harris, Andy [R-MD-1], Rep. Jones, Walter B., Jr. [R-NC-3], Rep. Ellmers, Renee L. [R-NC-2], Rep. Pompeo, Mike [R-KS-4], Rep. Long, Billy [R-MO-7], Rep. Graves, Tom [R-GA-14], Rep. Valadao, David G. [R-CA-22], Rep. Yoder, Kevin [R-KS-3], Rep. Whitfield, Ed [R-KY-1], Rep. Hurt, Robert [R-VA-5], Rep. Brat, Dave [R-VA-7], Rep. Griffith, H. Morgan [R-VA-9], Rep. Fleischmann, Charles J. "Chuck" [R-TN-3], Rep. Rigell, E. Scott [R-VA-2], Rep. Kinzinger, Adam [R-IL-16], Rep. Barletta, Lou [R-PA-11], Rep. Shimkus, John [R-IL-15], Rep. Flores, Bill [R-TX-17], Rep. Walker, Mark [R-NC-6], Rep. Wittman, Robert J. [R-VA-1], Rep. Forbes, J. Randy [R-VA-4], Rep. Blum, Rod [R-IA-1], Rep. Hudson, Richard [R-NC-8], Rep. Kline, John [R-MN-2], Sen. Blackburn, Marsha [R-TN], Rep. Neugebauer, Randy [R-TX-19], Rep. Sanford, Mark [R-SC-1], Rep. Mooney, Alexander X. [R-WV-2], Rep. Goodlatte, Bob [R-VA-6], Rep. Holding, George [R-NC-2], Rep. Zinke, Ryan K. [R-MT-1], Rep. Emmer, Tom [R-MN-6], Rep. Collins, Chris [R-NY-27], Rep. Ribble, Reid J. [R-WI-8], Rep. Thornberry, Mac [R-TX-13], Rep. Young, Don [R-AK-At Large], Rep. Stivers, Steve [R-OH-15], Rep. Byrne, Bradley [R-AL-1], Rep. Rogers, Harold [R-KY-5], Rep. Heck, Joseph J. [R-NV-3], Rep. Murphy, Tim [R-PA-18], Rep. Grothman, Glenn [R-WI-6]

Subjects

Healthcare

Source updated

12 August 2025

Healthcare

Summary

FDA Deeming Authority Clarification Act of 2015 This bill amends the Federal Food, Drug, and Cosmetic Act to revise premarket review and reporting requirements for products deemed by the Food and Drug Administration (FDA) to be tobacco products. A product is not subject to premarket review by the FDA if it is introduced to market before that type of product is deemed a tobacco product. A person introducing a tobacco product that is substantially similar to a marketed product less than 21 months after that type of product is deemed a tobacco product must submit a report to the FDA on the similar product not later than 21 months after that type of product is deemed a tobacco product. (A report is required at least 90 days prior to introduction of a tobacco product that is substantially similar to a marketed product if that type of product has been deemed a tobacco product for 21 months or more.)

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 28 April 2015

    Introduced

    Referred to the House Committee on Energy and Commerce.

    Source: IntroReferral

  2. 28 April 2015

    Introduced

    Sponsor introductory remarks on measure. (CR E596)

    Source: IntroReferral

  3. 28 April 2015

    Introduced

    Introduced in House

    Source: IntroReferral

  4. 28 April 2015

    Introduced

    Introduced in House

    Source: IntroReferral

  5. 1 May 2015

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

Votes

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Versions

Documents

3 official files

Introduced in House (text)

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  • Introduced in House (text)

    Introduced in House · EN · 28 April 2015

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  • Introduced in House (PDF)

    Introduced in House · EN · 28 April 2015

    ViewDownloadOpen at official source

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  • Introduced in House

    summary · EN · 28 April 2015

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Sponsors

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Related records

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Sources

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