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Home » Identifying Products as Medical Devices: The FDA’s Rules
Identifying Products as Medical Devices: The FDA’s Rules
Companies can find it challenging to figure out the most efficient and compliant method to bring new medical devices to the U.S. market. A thorough understanding of the nuances involved in FDA regulation of new devices is necessary for companies to successfully launch new products in the U.S. without regulatory complications. Both regulatory and business factors must be considered.