eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Draft Guidance for Industry and Staff; Availability: Procedures for Handling Section 522 Postmarket Surveillance Studies
Draft Guidance for Industry and Staff; Availability: Procedures for Handling Section 522 Postmarket Surveillance Studies
Document ID:
FDA-2011-D-0514-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2011-20727
View Document:
Details Information
Document Subtype:
Notice of Availability
Received Date:
August 16 2011, at 12:00 AM Eastern Daylight Time
Start-End Page:
50740 - 50741
Page Count:
2
Comment Start Date:
August 16 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
November 14 2011, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
7
Advanced Medical Technology Association - Comment
Posted:
11/16/2011
ID:
FDA-2011-D-0514-0003
Comment Period Closed
Nov 14,2011 11:59 PM ET
RTI Biologics, Inc. - Comment
Posted:
12/09/2011
ID:
FDA-2011-D-0514-0004
Comment Period Closed
Nov 14,2011 11:59 PM ET
American College of Cardiology - Comment
Posted:
12/09/2011
ID:
FDA-2011-D-0514-0005
Comment Period Closed
Nov 14,2011 11:59 PM ET
Medical Imaging & Technology Alliance (MITA) - Comment
Posted:
12/09/2011
ID:
FDA-2011-D-0514-0007
Comment Period Closed
Nov 14,2011 11:59 PM ET
Cook Group, Inc. - Comment
Posted:
12/09/2011
ID:
FDA-2011-D-0514-0008
Comment Period Closed
Nov 14,2011 11:59 PM ET
Related Documents
Total:
0
No documents available.
Draft Guidance for Industry and Staff; Availability: Procedures for Handling Section 522 Postmarket Surveillance Studies
Details Information
Comments
View AllPosted: 11/16/2011 ID: FDA-2011-D-0514-0003
Nov 14,2011 11:59 PM ET
Posted: 12/09/2011 ID: FDA-2011-D-0514-0004
Nov 14,2011 11:59 PM ET
Posted: 12/09/2011 ID: FDA-2011-D-0514-0005
Nov 14,2011 11:59 PM ET
Posted: 12/09/2011 ID: FDA-2011-D-0514-0007
Nov 14,2011 11:59 PM ET
Posted: 12/09/2011 ID: FDA-2011-D-0514-0008
Nov 14,2011 11:59 PM ET
Related Documents