Thomas J. Quinn - Citizen Petition

This Other document was issued by the Food and Drug Administration (FDA)

For related information, Open Docket Folder


See attached file(s)



Thomas J Quinn Citizen Petition

Authors: cdrh
Reason Restricted: This attachment is restricted to show metadata only because it contains personally identifiable information data.

Thomas J Quinn Citizen Petition Redacted

View Attachment:

ID: FDA-2013-P-0997-0001

Document Information

Date Posted: Aug 30, 2013
Show More Details  

Submitter Information

Country: United States
Category: Individual Consumer


Comments Received*
It is my belief that the FDA should review and update regulations governing MRI devices within their authority. The advances and increased power levels that are...
Any effort to improve the safety of patients, operators and service providers of any medical device should be reviewed by the FDA and implemented as necessary...

Docket Information

This document is contained in
Related Dockets:
Related RINs: None
Related Comments:

* This count refers to the total comment/submissions received on this document, 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.