Leading Edge Technology with Apteryx XVWeb: Artificial Intelligence and Dental Imaging
Planet DDS
JUNE 2, 2021
Previously under Class III, which is the highest regulatory burden, a new device would need to meet a reasonable assurance of safety and receive a pre-market approval before it could be sold. This downclassification is believed to be a willingness by the FDA to consider how it regulates image analysis software. Conclusion.
98 
Let's personalize your content