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The FDA is responsible for protecting public health by regulating human drugs and biological products, animal drugs, medical devices, tobacco products, food (including animal food), cosmetics, and electronic products that emit radiation.
U.S. Food and Drug Administration.
Overview Regulated ProductFind Information about:Medical DevicesMedical devices such as bandages, contact lenses, first aid kits, pacemakers, and surgical instrumentsRadiation-Emitting Electronic ProductsRadiation-emitting products such as x-ray machines, microwave ovens, CD-ROMs, LEDs, and laser pointers6 more rows • 1 Dec 2021
This is because the distinction between approved and cleared is significant: While FDA-approved means that the FDA has decided that the benefits of the product outweigh the known risks and manufacturers have to submit a pre-market approval application\u2013as well as clinical testing results\u2013in order to get approved, FDA- ...
FDA Mission The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation's food supply, cosmetics, and products that emit radiation.
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People also ask

What does 'FDA approved' mean? "FDA approved" means that the agency has determined that the "benefits of the product outweigh the known risks for the intended use." Manufacturers must submit a premarket approval (PMA) application and the results of clinical testing in order to get approval.
The FDA is responsible for protecting public health by regulating human drugs and biological products, animal drugs, medical devices, tobacco products, food (including animal food), cosmetics, and electronic products that emit radiation.
food additives. infant formulas. other food products (although the U.S. Department of Agriculture plays a lead role in regulating aspects of some meat, poultry, and egg products)...Biologics, including: vaccines for humans. blood and blood products. cellular and gene therapy products. tissue and tissue products. allergenics.
What Is the Food and Drug Administration? The Food and Drug Administration (FDA) is a government agency established in 1906 with the passage of the Federal Food and Drugs Act.
The FDA regulates a wide range of products, including foods (except for aspects of some meat, poultry and egg products, which are regulated by the U.S. Department of Agriculture); human and veterinary drugs; vaccines and other biological products; medical devices intended for human use; radiation-emitting electronic ...

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