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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter H - Medical Devices |
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Part 801 - Labeling |
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Subpart C - Labeling Requirements for Over-the-Counter Devices |
| § 801.60 - Principal display panel. |
| § 801.61 - Statement of identity. |
| § 801.62 - Declaration of net quantity of contents. |
| § 801.63 - Medical devices; warning statements for devices containing or manufactured with chlorofluorocarbons and other class I ozone-depleting substances. |