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Date: 2011-09-26 00:30:44 Technology Premarket approval Medical device Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Quality management system Percutaneous Headway Medicine Food and Drug Administration Health		510(k) Summary Trade Name: Generic Name: Classification: Submitted By: Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 131,76 KB Share Document on Facebook

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