HR 485
104th Congress
House
Foreign Trade and International Finance
Commerce
EEC countries
East Asia
Europe
European Union
Export controls
Exports
Health
Japan
Marketing
Medical research
Medical supplies
Product safety
Science, Technology, Communications
To expand the authority for the export of devices.
Introduced: January 11, 1995
See on congress.gov
Everywhere this bill has been
4 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Feb 6, 1995
Referred to the Subcommittee on Health and Environment.
Jan 17, 1995
Referred to the Subcommittee on International Economic Policy and Trade.
Jan 11, 1995
Referred to the Committee on Commerce, and in addition to the Committee on International Relations for a period to be subsequently determined by the Speaker, in each case for consideratiion of such provisions as fall within the jurisdiction of the committee concerned.
Jan 11, 1995
Introduced in House
Plain-English 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.
What's happening now
Referred to the Subcommittee on Health and Environment.
Cosponsors
1