Haven't spent much time on it. This looks like the patents are expedited to enable getting a test to the point it can be evaluated by FDA. The epiphany that created the holy cow was about the time many companies (and myself) thought they had the go ahead to just sell a coved19 home test, that was clarified and stopped. There is no if.
As I see it now they will still need FDA, but expect that also would be expedited. Step 1 is coming up with prototype.
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