FDA Guidance Documents·· 原文未提供具体时分
Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile: Guidance for Industry and Food and Drug Administration Staff
Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile: 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：2024-01-08。官方主题：Premarket, 510(k)。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov