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  2. Childhood dementia - Wikipedia

    en.wikipedia.org/wiki/Childhood_dementia

    Childhood dementia is an umbrella group of rare, mostly untreatable neurodegenerative disorders that show symptoms before the age of 18. These conditions cause progressive deterioration of the brain and the loss of previously acquired skills such as talking, walking, and playing.

  3. Pulsed electromagnetic field therapy - Wikipedia

    en.wikipedia.org/wiki/Pulsed_electromagnetic...

    In 2004, a pulsed electromagnetic field system was approved by the FDA as an adjunct to cervical fusion surgery in patients at high risk for non-fusion. [6] On 8/9 September 2020 the FDA recommended to shift PEMF medical devices from the Class 3 category to a Class 2 status. [7]

  4. Responsive neurostimulation device - Wikipedia

    en.wikipedia.org/wiki/Responsive_neuro...

    Responsive neurostimulation device is a medical device that senses changes in a person's body and uses neurostimulation to respond in the treatment of disease. The FDA has approved devices for use in the United States in the treatment of epileptic seizures [ 1 ] and chronic pain [ 2 ] conditions.

  5. How a new FDA-approved drug can — and can’t — help people ...

    www.aol.com/fda-approved-drug-t-help-121600044.html

    In early 2023, the U.S. Food and Drug Administration (FDA) granted accelerated approval to a new Alzheimer’s drug called Leqembi. (Biogen, a biotechnology company, and Eisai, a pharmaceutical ...

  6. Food and Drug Administration Amendments Act of 2007

    en.wikipedia.org/wiki/Food_and_Drug...

    It requires the FDA to submit an annual report to congressional committees that includes: (1) the number of devices approved in the preceding year for which there is a pediatric subpopulation that suffers from the disease; (2) the number of approved devices labeled for use in pediatric patients; (3) the number of fee-exempt devices approved ...

  7. Children’s National Hospital, Additional Ventures offer ...

    lite.aol.com/tech/story/0022/20240821/9218352.htm

    WASHINGTON, Aug. 21, 2024 (GLOBE NEWSWIRE) -- The Alliance for Pediatric Device Innovation (APDI), a nonprofit consortium led by Children’s National Hospital and funded by the Food and Drug Administration (FDA), announces today it is partnering with Additional Ventures, a nonprofit foundation focused on accelerating research progress and improving clinical care for individuals born with ...

  8. Paro (robot) - Wikipedia

    en.wikipedia.org/wiki/Paro_(robot)

    [3] [4] Paro was classified as a Class 2 medical device by U.S. regulators in fall 2009. [2] Paro has been used primarily in care facilities, especially as a form of therapy for dementia patients. [5] After a study was conducted to see the effects of robots on children with autism spectrum disorder, it appeared that there are numerous benefits ...

  9. FDA takes first step to protect children from medications ...

    www.aol.com/news/fda-takes-first-step-protect...

    The FDA called a meeting of experts to discuss how to define candy-like medicines including gummy vitamins and over-the-counter sleep aids. FDA takes first step to protect children from ...