| http://www.w3.org/ns/prov#value | - If the article is a drug within the general definition of 201 of the Federal Food, Drug, and Cosmetic Act (52 Stat. 1040, 21 U.S.C. 321 (1964 ed., Supp. II)), then the Secretary can subject it to pre-market clearance regulations [394 U.S. 784, 785]
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