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Implementation of Device Registration and Listing Requirements Enacted in the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, the Medical Device User Fee and Modernization Act of 2002, and Title II of the Food and Drug Administration Amendments Act of 2007

Document ID: FDA-2009-N-0114-0008
Document Type: Rule
Agency: Food And Drug Administration
Topics: Confidential Business Information, Imports, Medical Devices, Reporting and Recordkeeping Requirements
Federal Register Number: 2012-18764
CFR Citation: 21 CFR Part 807
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Details Information

Document Subtype: Final Rule
Received Date: August 02 2012, at 12:00 AM Eastern Daylight Time
Start-End Page: 45927 - 45944
Page Count: 18

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