FDA Guidance Documents·· 原文未提供具体时分
Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling : Guidance for Industry and Food and Drug Administration Staff
Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling : Guidance for Industry and Food and Drug Administration Staff
AI 导读
FDA 官方历史目录记录；Final guidance；发布日期：2015-03-17。官方主题：Premarket, 510(k), Investigational Device Exemption (IDE), Premarket Approval (PMA)。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov