1. 公告Medical Device Recall, FY2003-FY2012。
2. 公告草案指引(Draft Guidance)：Premarket Notification [510(k)] Submissions for Bipolar Electrosurgical Vessel Sealers for General Surgery、Premarket Assessment of Pediatric Medical Devices - Guidance for Industry and Food and Drug Administration Staff、Medical Device Tracking - Guidance for Industry and Food and Drug Administration Staff
3. 消費者資訊公告[對抗糖尿病的指引說明]。
參考資料：
U.S. FDA CDRHNews http://www.fda.gov/MedicalDevices/NewsEvents/News/default.htm#
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