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Nearly 4,500 cases were pulled from shelves in 23 states after it was found that the affected cans had been mislabeled.
By Stephanie Brown HealthDay ReporterMONDAY, May 19, 2025 (HealthDay News) -- Last week, the U.S. Food and Drug ...
The FDA has granted 510(k) marketing clearance to the first in vitro blood-based biomarker diagnostic device for Alzheimer’s ...
The U.S. Food and Drug Administration (FDA) has cleared marketing for a new blood test to diagnose Alzheimer's disease in ...
Japan-based Fujirebio's test, which helps doctors diagnose Alzheimer's disease, is intended for patients with signs of ...
The US Food and Drug Administration has given marketing clearance to a blood test to help diagnose Alzheimer’s disease, ...
The US Food and Drug Administration has cleared the first-ever blood test for diagnosing Alzheimer's disease, offering a less ...
The agency is planning a new review process that could result in ingredient bans or additional labeling requirements, ...
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ValleyCentral.com on MSNFDA approves first-ever Alzheimer’s blood testA few days ago, the U.S. Food and Drug Administration (FDA) cleared the first blood test to help detect early stages of ...
US Food and Drug Administration Commissioner Marty Makary named agency veterans to lead tobacco regulation and inspections, ...
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