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.
Introduced in House
Introduced in House
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.
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.
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.
Referred to the Subcommittee on International Economic Policy and Trade.
Referred to the Subcommittee on Health and Environment.
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