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Medical device / Premarket approval / Center for Devices and Radiological Health / Catheter / Title 21 of the Code of Federal Regulations / Percutaneous / Medtronic / Embolectomy / Atrial septal defect / Medicine / Health / Food and Drug Administration


y~i43JUN 510(k) Summary Submitter: Medtronic Vascular
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Document Date: 2012-07-06 14:44:48

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File Size: 144,60 KB

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