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FDA To Update Clearance Procedures For Medical Devices

News | January 7, 2019

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On November 26, 2018, the U.S. Food and Drug Administration (FDA) announced it was updating its 510(k) program clearance procedures for medical devices to ensure that new medical devices account for advances in technology or demonstrate that they meet more modern safety and performance criteria. The FDA intends to modernize the program by using more…

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