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General Provisions
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Medical Devices
Banned Devices
General Provisions
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Section
895.1
Scope.
Section
895.20
General.
Section
895.21
Procedures for banning a device.
Section
895.22
Submission of data and information by the manufacturer, distributor, or importer.
Section
895.25
Labeling.
Section
895.30
Special effective date.