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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-0114-0001
Document Type: Proposed Rule
Agency: Food And Drug Administration
Topics: Imports, Medical Devices, Reporting and Recordkeeping Requirements
Federal Register Number: 2010-06662
CFR Citation: 21 CFR Part 807
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Details Information

Document Subtype: NPR-Notice of Proposed Rule-Making
Received Date: March 26 2010, at 10:35 AM Eastern Daylight Time
Start-End Page: 14510 - 14538
Page Count: 29

Comments

   
Total: 3
Coastal Life Technologies (CLT), Inc. - Comment
Posted: 06/29/2010     ID: FDA-2009-N-0114-0005

Medline Industries, Inc. - Comment
Posted: 07/15/2010     ID: FDA-2009-N-0114-0006

Advanced Medical Techniology Association (AdvaMed) - Comment
Posted: 09/13/2010     ID: FDA-2009-N-0114-0007

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