1. 更新510(k) Submission Process說明，包括Log-in and Acknowledgement Process、Acceptance Review、Substantive Review、510(k) Decision Letter、Timeline of Communication with 510(k) Applicants。
2. 公告兩份指引草案(Draft Guidance)：Blood Glucose Monitoring Test Systems for Prescription Point-of-Care Use、Self-Monitoring Blood Glucose Test Systems for Over-the-Counter Use。
3. 諮議委員會：2014/2/20 Anesthesiology and Respiratory Therapy Devices Panel of the Medical Devices Advisory Committee Meeting Announcement。
4. 公告Automatic Class III Designation (De Novo)的評估方式。
5. FDA Voice Blog新增「Setting the Bar for Blood Glucose Meter Performance」。
6. 公告2013年9月及10月份PMA Final Decisions。
參考資料：
U.S. FDA CDRHNews http://www.fda.gov/MedicalDevices/NewsEvents/News/default.htm#
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