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Health / 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 / Unique Device Identification / Investigational Device Exemption / Food and Drug Administration / Medicine / Technology


P090003 Express® LD Iliac Premounted Stent System
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Document Date: 2013-12-06 12:12:06

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File Size: 167,06 KB

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