1. Design considerations and pre-market submission recommendations for interoperable medical devices: guidance for industry and Food and Drug Administration staff Publication: Silver Spring, MD : Center for Devices and Radiological Health, September 6, 2017 Subject(s): Equipment and Supplies -- standardsEquipment Design -- standardsEquipment Safety -- standardsDevice ApprovalEquipment FailureInformation DisseminationRisk ManagementHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
