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 » FDA Asks IOM to Evaluate 510(k) Clearance Process
FDA Asks IOM to Evaluate 510(k) Clearance Process
September 25, 2009
A $1.3 million review of the 510(k) clearance process being conducted by the Institute of Medicine (IOM) at the FDA’s request to determine if improvements are needed to protect patients is playing to mixed reactions in the device industry.