FDA Guidance Documents·· 原文未提供具体时分
Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, as amended – Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices: Guidance for Industry and FDA Staff
Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, as amended – Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices: Guidance for Industry and FDA Staff
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FDA 官方历史目录记录；Final guidance；发布日期：2006-05-01。官方主题：Postmarket, User Fees, Labeling。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov