2000 CFR Title 24, Volume 3

Title 21--Food and Drugs CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES PART 801--LABELING
	801.1	Medical devices; name and place of business of manufacturer, packer or distributor.
	801.4	Meaning of ``intended uses.''
	801.5	Medical devices; adequate directions for use.
	801.6	Medical devices; misleading statements.
	801.15	Medical devices; prominence of required label statements.
	801.16	Medical devices; Spanish-language version of certain required statements.
	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.
	801.109	Prescription devices.
	801.110	Retail exemption for prescription devices.
	801.116	Medical devices having commonly known directions.
	801.119	In vitro diagnostic products.
	801.122	Medical devices for processing, repacking, or manufacturing.
	801.125	Medical devices for use in teaching, law enforcement, research, and analysis.
	801.127	Medical devices; expiration of exemptions.
	801.150	Medical devices; processing, labeling, or repacking.
	801.405	Labeling of articles intended for lay use in the repairing and/or refitting of dentures.
	801.410	Use of impact-resistant lenses in eyeglasses and sunglasses.
	801.415	Maximum acceptable level of ozone.
	801.417	Chlorofluorocarbon propellants.
	801.420	Hearing aid devices; professional and patient labeling.
	801.421	Hearing aid devices; conditions for sale.
	801.430	User labeling for menstrual tampons.
	801.430	User labeling for menstrual tampons.
	801.433	Warning statements for prescription and restricted device products containing or manufactured with chlorofluorocarbons or other ozone-depleting substances.
	801.435	User labeling for latex condoms.
	801.437	User labeling for devices that contain natural rubber.