The Secretary of Health and Human Services shall annually post on the Internet Web site of the Food and Drug Administration—
(1)the number and type of class I and class II devices reclassified as class II or class III in the previous calendar year under section
360c(e)(1) of this title;
(2)the number and type of class II and class III devices reclassified as class I or class II in the previous calendar year under such section
360c(e)(1) of this title; and
(3)the number and type of devices reclassified in the previous calendar year under section
360e of this title.
The Secretary of Health and Human Services shall annually post on the Internet Web site of the Food and Drug Administration—
(1)the number and type of class I and class II devices reclassified as class II or class III in the previous calendar year under section
360c(e)(1) of this title;
(2)the number and type of class II and class III devices reclassified as class I or class II in the previous calendar year under such section
360c(e)(1) of this title; and
(3)the number and type of devices reclassified in the previous calendar year under section
360e of this title.
Section was enacted as part of the Food and Drug Administration Safety and Innovation Act and not as part of the Federal Food, Drug, and Cosmetic Act which comprises this chapter.
Section is comprised of subsec. (c) ofsection
608 of Pub. L. 112–144. Subsecs. (a) and (b) ofsection
608 amended sections
351,
360c to
360e, and
360g of this title and enacted provisions set out as notes under sections
351 and
360c of this title.
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