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  2. The FDA granted 510(k) clearance to Medtronic plc's (NYSE: MDT) LINQ II Insertable Cardiac Monitor (ICM) system for use in pediatric patients over the age of 2 who have heart rhythm abnormalities ...

  3. Humanitarian Device Exemption - Wikipedia

    en.wikipedia.org/wiki/Humanitarian_Device_Exemption

    A Humanitarian Device Exemption is an approval process provided by the United States Food and Drug Administration allowing a medical device to be marketed without requiring evidence of effectiveness. The FDA calls a device approved in this manner a "Humanitarian Use Device" (HUD).

  4. Ventricular assist device - Wikipedia

    en.wikipedia.org/wiki/Ventricular_assist_device

    The smallest device approved by the FDA, the HeartMate II, weighs about 1 pound (0.45 kg) and measures 3 inches (7.6 cm). This has proven particularly important for women and children, for whom alternatives would have been too large. [45] As of 2017, HeartMate III has been approved by the FDA.

  5. Winners announced in $300,000 pediatric medical device ...

    lite.aol.com/tech/story/0022/20241015/9256651.htm

    The competition is presented by the Alliance for Pediatric Device Innovation (APDI), a nonprofit consortium led by Children’s National Hospital and funded through the Food and Drug Administration (FDA), and Additional Ventures, a nonprofit focused on accelerating research progress and improving clinical care for individuals born with single ...

  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. US FDA approves Sanofi-AstraZeneca's preventive RSV ... - AOL

    www.aol.com/news/us-fda-approves-sanofi-astra...

    US FDA approves Sanofi-AstraZeneca's preventive RSV therapy for babies. July 17, 2023 at 1:06 PM ... around 1% to 3% of children under 12 months of age in the country are hospitalized each year ...

  9. New drug to protect babies and toddlers from RSV gets FDA ...

    www.aol.com/news/drug-protect-babies-toddlers...

    The Food and Drug Administration approved the injection for infants and children up to 2 years old who face increased risk of severe RSV. New drug to protect babies and toddlers from RSV gets FDA ...