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Labeling Requirements for Over-the-Counter Devices
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Medical Devices
Labeling
Labeling Requirements for Over-the-Counter Devices
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Section
801.60
Principal display panel.
Section
801.61
Statement of identity.
Section
801.62
Declaration of net quantity of contents.
Section
801.63
Medical devices; warning statements for devices containing or manufactured with chlorofluorocarbons and other class I ozone-depleting substances.