FDA Issues 2011 Plan To Improve the 510(k) Process
January 20, 2011
On January 19, 2011, the U.S. Food and Drug Administration (FDA) issued a plan containing 25 actions it intends to implement throughout 2011 to improve the 510(k) process, the most common path to market for medical devices. The FDA's goal is to support innovation in the medical device marketplace.
Access the press release here.