"Provides regulatory advice and support to the FDA’s regulatory review of digital health technology and is not responsible for making marketing authorization decisions."
Medical device reports submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters such as health care professionals, patients and consumers.
Provides safety information for radiological products used in medical imaging, surgery, security systems, home and business, entertainment, and tanning.
Contains a list of all medical devices with their associated classifications, product codes, FDA Premarket Review organizations, and other regulatory information.
The best place to learn about American patents and trademarks; the patent and appeals process ; the history of the USPTO; and the enforcement of intellectual property laws.