HR 6117
  • Introduced
    Nov 18, 2025
  • Passed House
  • Passed Senate
  • Signed into Law
HR 6117
United States House Bill
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To amend the Federal Food, Drug, and Cosmetic Act to authorize requiring the manufacturers of a covered device to disclose to a patient all patient-specific data that is recorded or transmitted by the device and accessible to the manufacturer, and for other purposes.
Last Action See all actions
House • Nov 18, 2025: Referred to the House Committee on Energy and Commerce.

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  • Nov 18, 2025 | House
    • Introduced in House
    • Referred to the House Committee on Energy and Commerce.
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