United States · Bill · HR
H.R. 485 (104th)
To expand the authority for the export of devices.
Introduced
11 January 1995
Last action
—
Status
Referred to the Subcommittee on Health and Environment.
Sponsors
—
Subjects
Discovery layer
Source updated
3 June 2026
Summary
Requires the Secretary of Health and Human Services, in administering a specified provision of the Federal Food, Drug, and Cosmetic Act, to make a determination, based on either of two specified notices concerning the approval of a medical device for marketing or investigational use in the European Community or by the Ministry of Health and Welfare of Japan, that the exportation of such medical device is not contrary to public health and safety, and has the approval of the importing country.
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Documents
3 official files
Introduced in House (text)
Introduced in House (text)
Introduced in House · EN · 11 January 1995
Introduced in House (PDF)
Introduced in House · EN · 11 January 1995
Introduced in House
summary · EN · 11 January 1995
Sponsors
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Related records
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Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://www.congress.gov/bill/104th-congress/house-bill/485
- Open data entity: https://api.congress.gov/v3/bill/104/hr/485