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 » U.S. FDA Issues Guidance for Cord Blood Processing, Storage Devices
U.S. FDA Issues Guidance for Cord Blood Processing, Storage Devices
March 6, 2007
A recently published U.S. Food and Drug Administration (FDA) guidance provides detailed information on what firms need to include in premarket notification, or 510(k), applications for cord blood processing systems and storage containers.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor