smart weight scales

By Brian Dolan 06:54 am August 1, 2014
Kinsa's smartphone-connected thermometer The US Food and Drug Administration has proposed to largely deregulate a sizable list of Class II and Class I medical devices and no longer require their makers to go through the 510(k) process. The agency made clear the deregulatory move would not necessarily exempt the device makers from other steps like appropriately registering and labeling their...