FDA, Assessment of Radiofrequency-Induced Heating in the Magnetic Resonance (MR) Environment for Multi-Configuration Passive Medical Devices, 2016
FDA, Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment, 2021
FDA, Non-Clinical Engineering Tests and Recommended Labeling for Intravascular Stents and Associated Delivery Systems, 2010
FDA, Intravascular Administration Sets Premarket Notification Submissions [510(k)], 2008
FDA, Medical Devices with Sharps Injury Prevention Features, 2005
FDA, Implantable Radiofrequency Transponder System for Patient Identification and Health Information, 2004
FDA, Implantable Middle Ear Hearing Device, 2003
FDA, Cardiovascular Intravascular Filter 510(k) Submissions, 1999
American College of Radiology, ACR Guidance Document on MR Safe Practices: 2013
Joint Commission, Preventing accidents and injuries in the MRI suite, Issue 38, 2008