Unique Device Identification for Postmarket Surveillance and Enforcement; Public Workshop

 
Docket ID: FDA-2011-N-0495
Agency: Food and Drug Administration (FDA)
Parent Agency: Department of Health and Human Services (HHS)
Summary:
Public workshop will be held September 12-13, 2011
Docket Details open glossary dialog  
Related RINs: None
Related Dockets: None
Short Title: Unique Device Identification for Postmarket Surveillance and Enforcement; Public Workshop
Keyword(s): CDRH201176, CDRH, Postmarket Surveillance, Enforcement
Type: Nonrulemaking
Docket Status: OPEN
Center: CDRH
Docket Item Code: N
 

Primary Documents

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Comment Period Closed
Oct 13, 2011 11:59 PM ET
Notice
Posted: 07/21/2011
ID: FDA-2011-N-0495-0001

Supporting Documents

 
No documents available.

Comments

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2
Comments Received*
*This count refers to the total comment/submissions received on this docket, as of 11:59 PM yesterday. Note: Agencies review all submissions, however some agencies may choose to redact, or withhold, certain submissions (or portions thereof) such as those containing private or proprietary information, inappropriate language, or duplicate/near duplicate examples of a mass-mail campaign. This can result in discrepancies between this count and those displayed when conducting searches on the Public Submission document type. For specific information about an agency’s public submission policy, refer to its website or the Federal Register document.