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Forgot to mention also, the FDA 510(K) clearance f

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Post# of 22465
(Total Views: 406)
Posted On: 06/26/2021 5:44:31 AM
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Posted By: Puravida19
Re: Puravida19 #20169
Forgot to mention also, the FDA 510(K) clearance for a non-covid testing device and platform using QD - That's big. QMC manufacturing? Seems so.

That device could well be in every emergency ward, doctor's office and clinical trial giving near instantaneous results on diseases, both qualitatively and quantitatively and all connected to a customized QMC HealthID for those purposes, in their respective ecosystems. Think Tricorder, although primitive in terms of Star Trek standards.

Why is QMC manufacturing this device instead of Innova? Innova makes tests, and this testing platform would be a logical extension. QMC does manufacture the QD for the tests and has the DLT HealthID for it, and its possible Squires had a hand in designing it because he knows the arena very well. One possible conclusion is that Innova wants QMC to do well so that its stock price rises for uplisting and just making money for Innova's pending 51% ownership.


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