Palo Alto, CA -- April 20, 2022 --Mobile authentication pioneer Incognia, today announced the launch of a new location identity fraud detection module to support mobile app security for customers ...
FCC adopted a Notice of Proposed Rulemaking which would relax the rules on conditional sales and imports of RF devices prior to authorization. Comments are due February 11 and Reply Comments are due ...
As a result of the COVID-19 pandemic, protective medical equipment including masks and gowns, and medical devices for use in testing and treating COVID-19 patients are in high demand. Manufacturers of ...
SALT LAKE CITY--(BUSINESS WIRE)--Spectrum Solutions, LLC today announced the U.S. Food and Drug Administration (FDA) has extended its Emergency Use Authorization for the SDNA-1000 Saliva Collection ...
During the COVID-19 public health emergency, the FDA has used its emergency use authorization to allow the use of unapproved medical devices or unapproved uses of authorized medical devices to combat ...
During its July 2017 Open Meeting, the Federal Communications Commission (FCC) voted to approve a Report and Order (R&O) containing new rules that impact how RF equipment, manufacturers, vendors, ...
SILVER SPRING, Md., Dec. 21, 2021 /PRNewswire/ -- Today, the U.S. Food and Drug Administration authorized marketing of the first laser-based device for the removal of Inferior Vena Cava (IVC) filters.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback