U.S. FDA Medical Device Update
Everyone, This is a very important regulatory update: U.S. FDA Medical Device Update US Food and Drug Administration medical device user fees for 510(k) premarket notifications, Premarket Approvals (PMAs) and other market registration applications will increase by about six percent for the agency’s 2020 fiscal year. FDA’s 2020 user fee schedule takes effect October 1, 2019, and entails six-percent […]
