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Technology / Center for Devices and Radiological Health / Premarket approval / 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 / Health


P080018 KODAK DirectView CR Mammography System
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Document Date: 2013-12-05 19:49:16

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File Size: 203,76 KB

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