1. Recommended content and format of non-clinical bench performance testing information in premarket submissions: guidance for industry and Food and Drug Administration staff Publication: Silver Spring, MD : Center for Devices and Radiological Health, December 20, 2019 Subject(s): Device Approval -- standardsMaterials Testing -- standardsEquipment and Supplies -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
