FDA Center for Devices and Radiological Health

23andMe gets FDA's go-ahead to sell genetic health risk tests, opening the door for faster approval for future tests
By Heather Mack | 04:35 pm | April 07, 2017
FDA recognizes device interoperability standards, potentially smoothing 510(k) reviews
By Neil Versel | 06:11 am | August 13, 2013