FDA Explains the Role of Mammography Facilities in Medical Device Reporting

Did you know that the Food and Drug Administration conducts post-market surveillance of medical devices, including mammography equipment? The Safe Medical Device Act of 1990 and the final Medical Device Reporting (MDR) rules published in 1995 imposed reporting requirements on the medical device industry, importers, and medical device user facilities, which includes mammography facilities. Continue reading »
Source: American College of Radiology - Category: Radiology Source Type: news