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USA guidances
U.S. Food and Drug Administration, Assessment of Radiofrequency-Induced Heating in the Magnetic Resonance (MR) Environment for Multi-Configuration Passive Medical Devices, 2016
U.S. Food and Drug Administration, Establishing Safety and Compatibility of Passive Implants in the Magnetic Resonance (MR) Environment, 2014
U.S. Food and Drug Administration, Non-Clinical Engineering Tests and Recommended Labeling for Intravascular Stents and Associated Delivery Systems, 2010
U.S. Food and Drug Administration, Intravascular Administration Sets Premarket Notification Submissions [510(k)], 2008
U.S. Food and Drug Administration, Medical Devices with Sharps Injury Prevention Features, 2005
U.S. Food and Drug Administration, Implantable Radiofrequency Transponder System for Patient Identification and Health Information, 2004
U.S. Food and Drug Administration, Implantable Middle Ear Hearing Device, 2003
U.S. Food and Drug Administration, Cardiovascular Intravascular Filter 510(k) Submissions, 1999
