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Overview of Device Regulation | FDA

    https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/overview-device-regulation
    The basic regulatory requirements that manufacturers of medical devices distributed in the U.S. must comply with are: Establishment registration, Medical Device Listing, Premarket Notification 510 (k), unless exempt, or Premarket Approval …

Medical Devices | FDA - U.S. Food and Drug Administration

    https://www.fda.gov/Medical-Devices
    Approvals and clearances, information on medical devices by type Digital Health Center of Excellence Cybersecurity, mobile medical apps, wireless medical devices, AI/ML in …

Medical Device Regulation comes into application

    https://www.ema.europa.eu/en/news/medical-device-regulation-comes-application
    Medical Device Regulation comes into application. Regulation (EU) 2017/745 on medical devices becomes applicable in the European Union today, 26 May 2021. The …

2022 medical device regulatory guidance plans from …

    https://www.emergobyul.com/news/us-fda-maps-out-medical-device-regulatory-guidance-planned-2022
    CDRH also plans new draft guidances on the FDA Breakthrough Devices Program; manufacturers’ reporting obligations related to medical device shortages under Section 506J of the Federal …



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