1. US Food & Drug Administration. Self—monitoring blood glucose test systems for over—the—counter use—guidance for industry and food and drug administration staff. Date unknown. https://www.fda.gov/. Accessed April 13, 2022.
2. US Food & Drug Administration. About manufacturer and user facility device experience (MAUDE). Date unknown. https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude#:~:text=Manufacturer%20and%20User%20Facility%20Device%20Experience%20(MAUDE)%20database%20represents%20reports,device%20report%20(MDR)%20data. Accessed April 13, 2022.