Search
Searching Content by J. Brennan from Foley Hoag LLP ordered by Published Date Descending.
Links to Result pages
 
1  
 
Title
Country
Organisation
Author
Date
1
FDA Releases Proposed Medical Device Reforms
In response to protracted public and political criticism of the Food and Drug Administration’s (FDA or Agency) regulation and review of medical devices under the premarket notification, or 510(k), process, the FDA’s Center for Devices and Radiological Health (CDRH or Center) yesterday released a set of proposed reforms to better "foster medical device innovation and assure the safety and effectiveness of medical technology."
United States
21 Jan 2011
Links to Result pages
 
1