AI-Powered Device Cleared as Noninvasive Skin Cancer Test
The handheld tool, intended for use by primary care physicians, uses spectroscopy and algorithms to evaluate skin lesions for potential cancer in a matter of seconds.
Source: medscape.com
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Dermasensor granted FDA clearance for skin cancer ID
Dermasensor Inc. received U.S. FDA clearance for its non-invasive skin cancer evaluation device that provides quantitative identification of all skin cancer types at the point of care and within seconds. The point-and-click device is designed to facilitate detection of skin cancers by primary care physicians (PCPs) and speed the time to diagnosis and treatment.
Source: bioworld.com
FDA Approves AI Device That Spots Skin Cancer
The FDA has authorized the first artificial intelligence-powered medical device to help doctors detect the most common forms of skin cancer in patients.
Source: healthday.com
FDA approves first AI medical device to detect skin cancer
The first medical device powered by artificial intelligence and designed to help doctors catch skin cancer has been approved by the U.S. Food and Drug Administration.
Source: upi.com
FDA Roundup: January 16, 2024
/PRNewswire/ -- Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA announced an...
Source: prnewswire.com