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Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment: Guidance for Industry and Food and Drug Administration Staff

Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment: Guidance for Industry and Food and Drug Administration Staff

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FDA 官方历史目录记录;Final guidance;发布日期:2023-10-10。官方主题:Premarket, Labeling, Safety - Issues, Errors, and Problems。请通过官方原文与附件查阅文件。

来源:FDA Guidance Documents · fda.gov