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 is the typical timeline for FDA certification of medical devices?
Category：行業(yè)資訊 Date：2024-11-04 17:00:07 Author: Source:
Overall, timelines can be affected by the quality of the submission, the complexity of the device, and the FDA's current workload.

The typical timeline for FDA certification of medical devices can vary widely based on the type of submission:1.jpg

  1. 510(k) Submission: Generally takes about 3 to 6 months, but it can be longer if additional information is requested.

  2. PMA (Premarket Approval): This process is more complex and can take 6 months to several years, depending on the device's nature and the data required.

  3. De Novo Classification: Usually takes about 6 months, but similar to 510(k), it may extend if the FDA needs more information.

Overall, timelines can be affected by the quality of the submission, the complexity of the device, and the FDA's current workload.

Contact Us：

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