FDA approves AI-powered skin cancer-screening device
Briefly

Officials at the FDA approved DermaSensor's software after analyzing the results of a study, led by the Mayo Clinic, that involved testing the device at 22 different clinics.
The results of the study showed that the device had a sensitivity of 96 percent and a specificity of 97 percent in detecting skin cancer cases. Additionally, a separate study demonstrated that the device helped reduce the rate of missed skin cancer cases from 18 percent to nine percent, as reported by 108 physicians using the device.
Read at Theregister
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