Requesting enforcement of the premarket notification requirements of the Act, with respect to reprocessed single-use devices

Docket ID: FDA-2011-P-0150
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
Keyword(s): CDRH, MDUFMA 302.b, Electronsurgical Device
Type: Nonrulemaking
Docket Status: OPEN
Center: CDRH
Docket Item Code: P

Primary Documents

View All  (3)
Comment Period Closed
Posted: 04/11/2012
ID: FDA-2011-P-0150-0003
Comment Period Closed
Posted: 04/11/2011
ID: FDA-2011-P-0150-0002
Comment Period Closed
Posted: 04/11/2011
ID: FDA-2011-P-0150-0001

Supporting Documents

No documents available.


No comments posted.

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.