We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Industry to US FDA: More Guidance Needed on ‘New’ 510(k) Policies
Industry to US FDA: More Guidance Needed on ‘New’ 510(k) Policies
March 10, 2010
Devicemakers want the U.S. Food and Drug Administration (FDA) to clarify “unofficial policies” that are hampering the agency’s 510(k)
review process, they told the agency at a meeting on strengthening the process.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor