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Health / Premarket approval / Center for Devices and Radiological Health / Medical device / Federal Food /  Drug /  and Cosmetic Act / Title 21 of the Code of Federal Regulations / Adverse event / Investigational Device Exemption / Unique Device Identification / Food and Drug Administration / Medicine / Technology


Microsoft Word - P890003s285a001.Letter.Appr.doc
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Document Date: 2014-05-06 11:11:30


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File Size: 63,24 KB

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