y~i43JUN 510(k) Summary Submitter: Medtronic Vascular

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Date: 2012-07-06 14:44:48 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 Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 144,60 KB Share Document on Facebook

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