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rayank

04/20/20 10:53 AM

#1052 RE: moder #1051

CEMI already has "Emergency Use Authorization" but is not FDA "approved" yet. So the testing on CEMI is ready for use if still in emergency conditions.
"NovaBay said it will submit the fluorecare test kit to the U.S. Food and Drug Administration under Emergency Authorization Use"
Sometimes it is a bit confusing even though we have "an agreement with Shenzhen Microprofit Biotech Co. to become the exclusive U.S. distributor of a rapid, finger prick test to determine the presence of Covid-19 or a potential indication of antibody immunity to Covid-19."
Good luck