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» Draft Guidance for Industry; Availability: Applying Human Factors and Usability Engineering to Optimize Medical Device Design
Draft Guidance for Industry; Availability: Applying Human Factors and Usability Engineering to Optimize Medical Device Design
Document ID:
FDA-2011-D-0469-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2011-15570
View Document:
Details Information
Document Subtype:
Notice of Availability
Received Date:
June 21 2011, at 12:00 AM Eastern Daylight Time
Start-End Page:
36543 - 36544
Page Count:
2
Comment Start Date:
June 22 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
September 19 2011, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
24
Sanofi - Comment
Posted:
09/27/2011
ID:
FDA-2011-D-0469-0017
Comment Period Closed
Sep 19,2011 11:59 PM ET
Draeger Medical GmbH - Comment
Posted:
09/27/2011
ID:
FDA-2011-D-0469-0018
Comment Period Closed
Sep 19,2011 11:59 PM ET
Muriel Didier - Comment
Posted:
09/27/2011
ID:
FDA-2011-D-0469-0019
Comment Period Closed
Sep 19,2011 11:59 PM ET
Stryker - Comment
Posted:
09/27/2011
ID:
FDA-2011-D-0469-0020
Comment Period Closed
Sep 19,2011 11:59 PM ET
International Pharmaceutical Aerosol Consortium on Regulation and Science (IPAC-RS) - Comment
Posted:
09/27/2011
ID:
FDA-2011-D-0469-0023
Comment Period Closed
Sep 19,2011 11:59 PM ET
Related Documents
Total:
0
No documents available.
Draft Guidance for Industry; Availability: Applying Human Factors and Usability Engineering to Optimize Medical Device Design
Details Information
Comments
View AllPosted: 09/27/2011 ID: FDA-2011-D-0469-0017
Sep 19,2011 11:59 PM ET
Posted: 09/27/2011 ID: FDA-2011-D-0469-0018
Sep 19,2011 11:59 PM ET
Posted: 09/27/2011 ID: FDA-2011-D-0469-0019
Sep 19,2011 11:59 PM ET
Posted: 09/27/2011 ID: FDA-2011-D-0469-0020
Sep 19,2011 11:59 PM ET
Posted: 09/27/2011 ID: FDA-2011-D-0469-0023
Sep 19,2011 11:59 PM ET
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