To expand the authority for the export of devices.

[AI summary unavailable — showing source text] 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.…