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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 895 - Banned Devices |
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Subpart A - General Provisions |
| § 895.1 - Scope. |
| § 895.20 - General. |
| § 895.21 - Procedures for banning a device. |
| § 895.22 - Submission of data and information by the manufacturer, distributor, or importer. |
| § 895.25 - Labeling. |
| § 895.30 - Special effective date. |