FDA Guidance Documents·· 原文未提供具体时分
Policy Clarification and Premarket Notification [510(k)] Submissions for Ultrasonic Diathermy Devices: Guidance for Industry and Food and Drug Administration Staff
Policy Clarification and Premarket Notification [510(k)] Submissions for Ultrasonic Diathermy Devices: 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：2023-02-21。官方主题：Premarket, 510(k), Physical Medicine。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov