Today, the @US_FDA issued the final guidance: 510(k) Third Party Review Program and is updating the list of devices eligible for review under the 510(k) Third Party Review Program.pic.twitter.com/wI3inf5TM5

Today, the @US_FDA issued the final guidance: 510(k) Third Party Review Program and is updating the list of devices eligible for review under the 510(k) Third Party Review Program. pic.twitter.com/wI3inf5TM5

Source: Food and Drug Adminstration (FDA): CDRHNew - March 11, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news