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» General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device; Reopening of Comment Period
General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device; Reopening of Comment Period
Document ID:
FDA-2006-N-0178-0049
Document Type:
Proposed Rule
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
E8-21200
CFR Citation:
21 CFR 878
View Document:
Details Information
Document Subtype:
NEC-Notice of Extension
Received Date:
September 10 2008, at 07:53 AM Eastern Daylight Time
Start-End Page:
52804 - 52805
Page Count:
2
Comment Start Date:
September 11 2008, at 12:00 AM Eastern Standard Time
Comment Due Date:
October 14 2008, at 11:59 PM Eastern Standard Time
Comments
Total:
5
LifeScience Plus, Inc. - Comment
Posted:
09/29/2008
ID:
FDA-2006-N-0178-0051
Comment Period Closed
Oct 14,2008 11:59 PM ET
Baxter Healthcare Corporation - Comment
Posted:
10/15/2008
ID:
FDA-2006-N-0178-0052
Comment Period Closed
Oct 14,2008 11:59 PM ET
Ethicon, Inc. - Comment
Posted:
10/16/2008
ID:
FDA-2006-N-0178-0053
Comment Period Closed
Oct 14,2008 11:59 PM ET
Ferrosan A/S - Comment
Posted:
10/17/2008
ID:
FDA-2006-N-0178-0054
Comment Period Closed
Oct 14,2008 11:59 PM ET
Andrea Ortegon - Comment
Posted:
06/03/2010
ID:
FDA-2006-N-0178-0055
Comment Period Closed
Oct 14,2008 11:59 PM ET
Related Documents
Total:
2
General and Plastic Surgery Devices: Proposed Classification for the Tissue Expander
General and Plastic Surgery Devices; Reclassification of the Tissue Adhesive for Topical Approximation of Skin Device
General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device; Reopening of Comment Period
Details Information
Comments
Posted: 09/29/2008 ID: FDA-2006-N-0178-0051
Oct 14,2008 11:59 PM ET
Posted: 10/15/2008 ID: FDA-2006-N-0178-0052
Oct 14,2008 11:59 PM ET
Posted: 10/16/2008 ID: FDA-2006-N-0178-0053
Oct 14,2008 11:59 PM ET
Posted: 10/17/2008 ID: FDA-2006-N-0178-0054
Oct 14,2008 11:59 PM ET
Posted: 06/03/2010 ID: FDA-2006-N-0178-0055
Oct 14,2008 11:59 PM ET
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