USA FDA MR Guidances
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时间:2022-8-30 22:29:06
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FDA, Assessment of Radiofrequency-Induced Heating in the Magnetic Resonance (MR) Environment for Multi-Configuration Passive Medical Devices, 2016
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FDA, Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment, 2021
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FDA, Non-Clinical Engineering Tests and Recommended Labeling for Intravascular Stents and Associated Delivery Systems, 2010
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FDA, Intravascular Administration Sets Premarket Notification Submissions [510(k)], 2008
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FDA, Medical Devices with Sharps Injury Prevention Features, 2005
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FDA, Implantable Radiofrequency Transponder System for Patient Identification and Health Information, 2004
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FDA, Implantable Middle Ear Hearing Device, 2003
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FDA, Cardiovascular Intravascular Filter 510(k) Submissions, 1999