InvestorsHub Logo
Followers 0
Posts 1442
Boards Moderated 0
Alias Born 10/04/2017

Re: Door2Door post# 6555

Thursday, 12/28/2017 4:45:41 PM

Thursday, December 28, 2017 4:45:41 PM

Post# of 12427
And the FDA 510K accelerated path to market is why FDA clearance is such a shoe in. LXGTF has already provided early testing info that shows a correlation to ultrasound results re endothelial function. They dont have to reinvent the wheel with the clinicals, only establish that they are as good or better than precursor technology. Which is why I estimate no longer that 6 months from last November.