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» Agfa HealthCare - Comment
Agfa HealthCare - Comment
Document ID:
FDA-2008-N-0273-0006
Document Type:
Public Submission
Agency:
Food And Drug Administration
Received Date:
June 30 2008, at 01:45 PM Eastern Daylight Time
Date Posted:
July 18 2008, at 12:00 AM Eastern Standard Time
Comment Start Date:
May 30 2008, at 12:00 AM Eastern Standard Time
Comment Due Date:
August 28 2008, at 11:59 PM Eastern Standard Time
Tracking Number:
8064b7fb
View Document:
This is comment on Notice
Medical Devices; Radiology Devices; Reclassification of Full Field Digital Mammography System
View Comment
Agfa HealthCare supports the FDA's initiative to down classify Digital Mammography from Class III to Class II.
Related Comments
View All
Total:
12
Agfa HealthCare - Comment
Public Submission
Posted:
07/18/2008
ID:
FDA-2008-N-0273-0006
Comment Period Closed
Aug 28,2008 11:59 PM ET
The University of North Carolina School of Medicine - Comment
Public Submission
Posted:
07/18/2008
ID:
FDA-2008-N-0273-0007
Comment Period Closed
Aug 28,2008 11:59 PM ET
University of North Carolina at Chapel Hill - Comment
Public Submission
Posted:
08/26/2008
ID:
FDA-2008-N-0273-0009
Comment Period Closed
Aug 28,2008 11:59 PM ET
Agfa HealthCare Corporation - Comment
Public Submission
Posted:
08/28/2008
ID:
FDA-2008-N-0273-0012
Comment Period Closed
Aug 28,2008 11:59 PM ET
General Electric Healthcare - Comment
Public Submission
Posted:
08/28/2008
ID:
FDA-2008-N-0273-0013
Comment Period Closed
Aug 28,2008 11:59 PM ET
Agfa HealthCare - Comment
This is comment on Notice
Medical Devices; Radiology Devices; Reclassification of Full Field Digital Mammography System
View Comment
Related Comments
View AllPublic Submission Posted: 07/18/2008 ID: FDA-2008-N-0273-0006
Aug 28,2008 11:59 PM ET
Public Submission Posted: 07/18/2008 ID: FDA-2008-N-0273-0007
Aug 28,2008 11:59 PM ET
Public Submission Posted: 08/26/2008 ID: FDA-2008-N-0273-0009
Aug 28,2008 11:59 PM ET
Public Submission Posted: 08/28/2008 ID: FDA-2008-N-0273-0012
Aug 28,2008 11:59 PM ET
Public Submission Posted: 08/28/2008 ID: FDA-2008-N-0273-0013
Aug 28,2008 11:59 PM ET