高清不卡日本v二区在线,天天综合网天天综合,激情丁香五月天婷婷水蜜桃视频,91精品免费久久久久久久久,手机看片久久久久久久久,日日夜夜嫩草,日本不卡 在线视频,欧美亚洲日韩,高潮歹无毛免费观看视频,天天综合网7799日日夜夜永,欧美日本国产日韩激情视频 ,久久久无码精品亚洲日韩蜜桃,日夜夜天天人人综合网,91蜜桃长长久久,国产精品精品一区在线发布,一级a毛片免费观看久久精品

What Are the Common Timelines and Durations for FDA Certification Applications?
Category：行業(yè)資訊 Date：2024-09-14 16:34:58 Author: Source:
Each timeline can be influenced by factors such as the completeness of the application, the complexity of the device, and the FDA’s workload.

Common timelines and durations for FDA certification applications vary by type:8.jpg

  1. 510(k) Submission: Typically takes about 90 days, but can extend if additional information is required.
  2. Premarket Approval (PMA): Generally around 180 days, though it may be longer for complex devices or additional data requests.
  3. De Novo Request: Usually around 150 days, but can vary based on the specifics of the application.

Each timeline can be influenced by factors such as the completeness of the application, the complexity of the device, and the FDA’s workload.

Contact Us：

Whatsapp or Wechat：+86 15816864648；email address：hito.lin@grzan.cn