Veritract 510k Final - Round[removed] - Center for Devices and Radiological Health - Document - PDFSEARCH.IO

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Date: 2014-09-23 12:22:32 Health Center for Devices and Radiological Health Medical device Premarket approval Title 21 of the Code of Federal Regulations Federal Food Drug and Cosmetic Act Quality management system Code of Federal Regulations Title 21 CFR Part 11 Medicine Food and Drug Administration Technology		Veritract 510k Final - Round[removed] Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 68,24 KB Share Document on Facebook

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