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Date: 2003-05-28 09:55:52 Technology Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medical device Title 21 of the Code of Federal Regulations Design controls Adverse event Premarket approval Investigational Device Exemption Food and Drug Administration Medicine Health		Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 301,41 KB Share Document on Facebook

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