§ 360f. Banned devices
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/usc/title-21/section-360fA research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(a)General rule Whenever the Secretary finds, on the basis of all available data and information, that—
(1)a device intended for human use presents substantial deception or an unreasonable and substantial risk of illness or injury for one or more intended uses; and
(2)in the case of substantial deception or an unreasonable and substantial risk of illness or injury which the Secretary determined could be corrected or eliminated by labeling or change in labeling and with respect to which the Secretary provided written notice to the manufacturer specifying the deception or risk of illness or injury, the labeling or change in labeling to correct the deception or eliminate or reduce such risk, and the period within which such labeling or change in labeling was to be done, such labeling or change in labeling was not done within such period;
he may initiate a proceeding to promulgate a regulation to make such device a banned device or to make such intended use or uses a banned intended use or uses. A device that is banned for one or more intended uses is not a legally marketed device under section 396 of this title when intended for such use or uses.
(b)Special effective date The Secretary may declare a proposed regulation under subsection
(a)to be effective upon its publication in the Federal Register and until the effective date of any final action taken respecting such regulation if
(1)he determines, on the basis of all available data and information, that the deception or risk of illness or injury associated with the use of the device which is subject to the regulation presents an unreasonable, direct, and substantial danger to the health of individuals, and
(2)before the date of the publication of such regulation, the Secretary notifies the manufacturer of such device that such regulation is to be made so effective. If the Secretary makes a proposed regulation so effective, he shall, as expeditiously as possible, give interested persons prompt notice of his action under this subsection, provide reasonable opportunity for an informal hearing on the proposed regulation, and either affirm, modify, or revoke such proposed regulation.
(June 25, 1938, ch. 675, § 516, as added Pub. L. 94–295, § 2, May 28, 1976, 90 Stat. 560; amended Pub. L. 101–629, § 18(d), Nov. 28, 1990, 104 Stat. 4529; Pub. L. 117–328, div. FF, title III, § 3306(a), Dec. 29, 2022, 136 Stat. 5834.)
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public-private-law
U.S. Code
register
- Proposed RulesProposed amendment; proposed order
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- NoticesFinal rule
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- Proposed RulesAdvance notice of proposed rulemaking
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statutes-at-large
- Public Law 94–295To amend the Federal Food, Drug, and Cosmetic Act to provide for the safety and effectiveness of medical devices intended for human use, and for other purposes
- Public Law 101–629To amend the Federal Food, Drug, and Cosmetic Act to make improvements in the regulation of medical devices, and for other purposes
Traces to 4 documents
7 references not yet in our index
- June 25, 1938, ch. 675, § 516
- Pub. L. 94–295, § 2
- 90 Stat. 560
- Pub. L. 101–629, § 18(d)
- 104 Stat. 4529
- 136 Stat. 5834
- Pub. L. 101–629
Citation graph
cites case law
§ 360f
Banned devices
Fed. Reg.×74
Bills×12
U.S.C.×9
Stat.×5
Pub. L.×3
ActJune 25, 1938, ch. 675, § 516
Pub. L.Pub. L. 94–295, § 2
Stat.90 Stat. 560
Pub. L.Pub. L. 101–629, § 18(d)
Stat.104 Stat. 4529
Cites 11 · showing 9Cited by 103 across 5 sources