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» Draft Guidances for Industry and Staff: Refuse to Accept Policy for 510(k)s
Draft Guidances for Industry and Staff: Refuse to Accept Policy for 510(k)s
Document ID:
FDA-2012-D-0523-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2012-19744
View Document:
Details Information
Document Subtype:
Notice of Availability
Received Date:
August 13 2012, at 12:00 AM Eastern Daylight Time
Start-End Page:
48159 - 48160
Page Count:
2
Comment Start Date:
August 13 2012, at 12:00 AM Eastern Standard Time
Comment Due Date:
September 27 2012, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
7
Novo Nordisk - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0523-0006
Comment Period Closed
Sep 27,2012 11:59 PM ET
Abbott Laboratories - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0523-0007
Comment Period Closed
Sep 27,2012 11:59 PM ET
Advanced Medical Technology Association (AdvaMed) - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0523-0008
Comment Period Closed
Sep 27,2012 11:59 PM ET
Orthopedic Surgical Manufacturers Association (OSMA) - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0523-0009
Comment Period Closed
Sep 27,2012 11:59 PM ET
Medical Imaging and Technology Alliance (MITA) - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0523-0010
Comment Period Closed
Sep 27,2012 11:59 PM ET
Related Documents
Total:
0
No documents available.
Draft Guidances for Industry and Staff: Refuse to Accept Policy for 510(k)s
Details Information
Comments
View AllPosted: 10/02/2012 ID: FDA-2012-D-0523-0006
Sep 27,2012 11:59 PM ET
Posted: 10/02/2012 ID: FDA-2012-D-0523-0007
Sep 27,2012 11:59 PM ET
Posted: 10/02/2012 ID: FDA-2012-D-0523-0008
Sep 27,2012 11:59 PM ET
Posted: 10/02/2012 ID: FDA-2012-D-0523-0009
Sep 27,2012 11:59 PM ET
Posted: 10/02/2012 ID: FDA-2012-D-0523-0010
Sep 27,2012 11:59 PM ET
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