Ebola Test From J&J's Janssen Earns FDA Emergency Use Authorization

The FDA has issued emergency use authorization (EUA) for Johnson & Johnson (J&J) subsidiary Janssen’s real-time diagnostic device indicated for the Ebola Zaire virus, which was responsible for the 2014 outbreak in West Africa. Using only a few drops of blood, the device can deliver results in less than two hours, and its cartridges are designed for easy transit and safe disposal.
Source: Medical Design Online News - Category: Medical Equipment Source Type: news