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3 cosponsors · 1 D, 2 R
3 signed on when it was introduced; the rest joined later. Cosponsors who withdrew aren't shown.
- Senate Introduced Nov 18, 2003
- Senate Passed Nov 25, 2003
- House Passed Mar 10, 2004 396–0
- Senate Changes resolved Mar 12, 2004
- President To the President Mar 22, 2004
- President Signed Apr 1, 2004
- Law Apr 1, 2004
Medical Devices Technical Corrections Act - Amends the Federal Food, Drug, and Cosmetic Act (as amended by the Medical Device User Fee and Modernization Act of 2002) to revise provisions concerning medical devices user fees.
What it does: CRS summary · Public Law · Apr 1, 2004
(This measure has not been amended since it was reported to the House on March 9, 2004. The summary of that version is repeated here.)
Medical Devices Technical Corrections Act - Amends the Federal Food, Drug, and Cosmetic Act (as amended by the Medical Device User Fee and Modernization Act of 2002) to revise provisions concerning medical devices user fees.
Prohibits the Secretary of Health and Human Services from collecting fees to defray costs in any fiscal year where the amount appropriated is more than five percent below the costs of the resources allocated for the review of device applications.
Allows the Secretary to withdraw accreditation to inspect from any person where the Secretary determines that there is a conflict of interest between the company and the accredited inspector.
Permits a company that markets at least one medical device in the United States and one medical device in another country to use an accredited third party inspector if the company certifies that the foreign country recognizes inspections by: (1) the Food and Drug Administration (FDA); and/or (2) the third party inspector. (Current law requires a country to recognize both types of inspections.)
Allows the Secretary to withdraw eligibility for third party inspections from a company if the Secretary determines that the company is substantially not in compliance with the Act.
Allows electronic labeling for prescription devices intended for use by health care professionals and for in vitro diagnostic devices intended for use by health care professionals or in blood establishments.
Delays by 18 additional months the effective date of the provision deeming a device misbranded if the identification of the manufacturer is not conspicuously displayed.
Directs the Secretary to submit a report to the relevant committees on the barriers to the availability of devices intended for treatment or diagnosis of diseases or conditions that affect children.
Written by the nonpartisan Congressional Research Service. All summary versions on Congress.gov
Votes to become law
About this bill and sources
Official title: Medical Devices Technical Corrections Act
Latest action (Apr 1, 2004): Became Public Law No: 108-214.
Policy area: Health · Origin: Senate · Introduced: Nov 18, 2003
Official page on Congress.gov · Bill text (GovInfo) · Status record (XML) · Embed in your story
- Senate Introduced Nov 18, 2003
- Senate Passed Nov 25, 2003
- House Passed Mar 10, 2004 396–0
- Senate Changes resolved Mar 12, 2004
- President To the President Mar 22, 2004
- President Signed Apr 1, 2004
- Law Apr 1, 2004
Final vote · House · Mar 10, 2004
Passage (two-thirds required) — Passed. Vote details
Speaker of the House: J. Dennis Hastert