Strengthening the Center for Devices and Radiological Health’s 510(k) Review Process; Public Meeting; Request for Comments

 
Docket ID: FDA-2010-N-0054
Agency: Food and Drug Administration (FDA)
Parent Agency: Department of Health and Human Services (HHS)
Docket Details open glossary dialog  
Related RINs: None
Related Dockets: None
Type: Nonrulemaking
Center: CDER
Docket Item Code: N
 

Primary Documents

View All  (4)
Comment Period Closed
Mar 19, 2010 11:59 PM ET
Notice
Posted: 03/05/2010
ID: FDA-2010-N-0054-0009
Comment Period Closed
Mar 05, 2010 11:59 PM ET
Notice
Posted: 01/27/2010
ID: FDA-2010-N-0054-0001
Comment Period Closed
Other
Posted: 02/18/2010
ID: FDA-2010-N-0054-0003
Comment Period Closed
Other
Posted: 02/18/2010
ID: FDA-2010-N-0054-0004

Supporting Documents

 
No documents available.

Comments

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109
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.