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 Date: 2012-04-23 02:33:50Health Adverse event Premarket approval Medical device MedWatch Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Independent reviewer Food and Drug Administration Medicine Technology |
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http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSear