As the US faces a shortage of coronavirus tests, a new test to be used mainly in hospitals and emergency rooms was approved. Testing is considered a key part of efforts to limit the spread of the new coronavirus.
US regulators approved a fast coronavirus test on Saturday, in time to supply a nation that has struggled to meet test demand as the COVID-19 pandemic ramps up.
The test has a detection time of 45 minutes and was developed by California-based molecular diagnostics company Cepheid.
It gained approval from the US Food and Drug Administration (FDA) through emergency authorization and plans to begin shipping tests next week.
The tests will be primarily distributed at hospitals and emergency rooms.
"With new tools like point-of-care diagnostics, we are moving into a new phase of testing, where tests will be much more easily accessible to Americans who need them," US Secretary of Health and Human Services Alex Azar said.
Azar added the tests would provide "results within hours, rather than days like the existing tests."
These systems do not require users to have special training to operate and are capable of running around the clock, Cepheid President Warren Kocmond said in the statement.
"Point-of-care testing means that results are delivered to patients in the patient care settings, like hospitals, urgent care centers and emergency rooms, instead of samples being sent to a laboratory," FDA Commissioner Stephen Hahn said.
More than 19,000 COVID-19 infections have been confirmed in the US, with over 270 deaths. Some tens of millions of people are under lockdown measures in order to help curb the spread of the virus.