The Food and Drug Administration on Tuesday approved the first rapid at-home COVID-19 test. The FDA granted emergency use authorization to the 30-minute test kit from California-based manufacturer Lucira Health. The test is prescription-only and solely approved for those 14 and older. “This new testing option is an important diagnostic advancement to address the pandemic…
Source: NY Post click here for more…
First rapid at-home COVID-19 test approved by FDA
Published in New York City
More from New York CityMore posts in New York City »
- John Harbaugh isn’t worried about his Ravens job security with season nearly lost
- JD Vance trains with Navy SEALs in California: ‘Feel like I got hit by a freight train’
- It’s undeniable US allowed child trafficking during Afghan withdrawal — now’s the time to make it right
- Goodbye (and Good Riddance?) to the MetroCard
- Bernie Sanders to Lead Zohran Mamdani’s Public Swearing-In Ceremony
Be First to Comment