P080018 KODAK DirectView CR Mammography System

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Date: 2013-12-05 19:49:16 Technology Center for Devices and Radiological Health Premarket approval Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Health		P080018 KODAK DirectView CR Mammography System Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 203,76 KB Share Document on Facebook

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