Today we received final confirmation from FDA that KEWS300 is cleared for sale within the US. The user-centered design and extensive software validations, independently certified to the medical device software standard (ISO62304), allow us to offer this system to US-based customers with real confidence.
http://www.syncrophi.com/wp-content/uploads/2017/02/fda.jpg800800heaventreehttp://www.syncrophi.com/wp-content/uploads/2017/04/LOGO-SMALL.pngheaventree2017-02-13 14:19:542017-06-08 11:42:05KEWS300 now FDA-cleared
Where to find us
Syncrophi Systems Ltd
Racecourse Business Park