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 » Suggestions to Overhaul 510(k) Process Not All Necessary, Devicemakers Say
Suggestions to Overhaul 510(k) Process Not All Necessary, Devicemakers Say
August 12, 2010
The sheer number of suggestions included in a report aimed at overhauling the U.S. Food and Drug Administration’s (FDA) 510(k) clearance process is enough to give the device industry pause.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor