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Re: Door2Door post# 6781

Wednesday, 01/03/2018 8:00:41 AM

Wednesday, January 03, 2018 8:00:41 AM

Post# of 12427
Seems like the FDA agrees with me (as much as you could say that about a regulatory behemoth like that) which is why they have this in the 510 k accelerated path to market. One of the stipulations is that it is considered a medical breakthrough that saves lives.