US Food and Drug Administration Self-approval of COVID monitoring equipment at home

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US Food and Drug Administration Self-approval of COVID monitoring equipment at home

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The US Food and Drug Administration or ดาวน์โหลด SLOTXO FDA approves the use of a device to detect COVID-19. Get yourself at home for the first time Which can know the result within 20 minutes

FDA approves home use of a home-based rapid test for COVID-19 For emergency on Tuesday This is a major step forward in the non-prescription testing of COVID-19 in the United States.

Under the approval of the FDA, this will make Americans. Can be purchased for COVID-19 detection devices Can be said in pharmacies While the test was a nasal swab, the FDA confirmed that the results were 96% accurate to symptomatic infected people. And gave a low error in the group with asymptomatic infection Results can be seen quickly within 20 minutes via a smartphone application that is directly connected to the COVID test kit. And can contact the doctor immediately after knowing the results

Initial COVID-19 monitoring equipment This home is limited by Ellume, the maker of the COVID-19 test kit. Australian citizenship It is expected to produce about 3 million sets in the next month. And will expand production capacity in the first half of next year The price is 30 dollars or about 900 baht.

Last month, the FDA approved the use of a self-testing device for COVID-19, but requires a doctor's prescription to be able to purchase it at home. And previously the US Food and Drug Administration More than 225 types of COVID-19 testing have been approved since the COVID outbreak in the US. In the United States, about 2 million people are tested for the novel coronavirus per day. Which public health experts think is not enough

The latest situation in the US According to Johns Hopkins University, 16.6 million people have accumulated more than 300,000 deaths.

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