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
