The daily business briefing: November 18, 2020

The FDA approves the first at-home rapid coronavirus test, GOP defectors join Democrats to hold up Trump's Fed nominee, and more

An at-home COVID test
(Image credit: Leon Neal/Getty Images)

1. FDA approves first complete at-home rapid COVID-19 test

The Food and Drug Administration on Tuesday granted emergency use approval for the first rapid coronavirus test for complete use at home. The test, developed by California-based company Lucira Health, requires a prescription, and is expected to cost $50 or less. It relies on a nasal swab, and can provide results in half an hour. Other at-home tests that have already received FDA approval require samples to be shipped to a lab for analysis. Jeff Shuren, director of the FDA's Center for Devices and Radiological Health, said the authorization of a complete at-home test marks "a significant step" for the FDA's COVID-19 response. "Now, more Americans who may have COVID-19 will be able to take immediate action, based on their results, to protect themselves and those around them," Shuren said.

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Harold Maass, The Week US

Harold Maass is a contributing editor at The Week. He has been writing for The Week since the 2001 debut of the U.S. print edition and served as editor of TheWeek.com when it launched in 2008. Harold started his career as a newspaper reporter in South Florida and Haiti. He has previously worked for a variety of news outlets, including The Miami Herald, ABC News and Fox News, and for several years wrote a daily roundup of financial news for The Week and Yahoo Finance.