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


P980018/S010 HercepTestTM
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Document Date: 2013-12-06 12:10:14

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File Size: 163,33 KB

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