21 CFR Subpart C
Labeling Requirements for Over-the-Counter Devices
June 25, 2020
§
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
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