FDA digital health

FDA looks to restrict older predicate devices, introduce new regulatory pathway
By Dave Muoio | 02:34 pm | November 27, 2018
To encourage healthcare technology innovation and update the 510(k) pathway, the regulatory agency said that it will soon release measures aimed to sunset predicate devices that are over a decade old. 
FDA wellness clarifications helpful, accessory proposal is just a start
By Brian Dolan | 08:23 am | January 20, 2015
Verizon shutters Virtual Visits and its FDA-cleared telehealth hub app
By Brian Dolan | 07:07 am | January 12, 2015
LifeWatch gets FDA clearance for adhesive, remote patient monitoring wearable
By Jonah Comstock | 10:39 am | December 22, 2014