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 Costs and Timelines for FDA Certification of Medical Devices?
Category:行業(yè)資訊 Date:2024-09-14 16:33:10 Author: Source:
Additional costs may include clinical trials, testing, and consulting fees. Timelines can be influenced by the completeness of the application and the FDA’s review process.

The costs and timelines for FDA certification of medical devices vary based on the submission type:8(2).jpg

  1. 510(k) Submission:

    • Cost: Approximately $12,000 (for standard review); may be reduced for small businesses.
    • Timeline: Typically 90 days, but can be longer if additional information is requested.
  2. Premarket Approval (PMA):

    • Cost: Approximately $365,000 (for standard review); varies with the complexity of the device.
    • Timeline: Usually 180 days, but can be extended based on the need for additional data or complex reviews.
  3. De Novo Request:

    • Cost: Approximately $13,000.
    • Timeline: Generally around 150 days, but may vary based on submission specifics.

Additional costs may include clinical trials, testing, and consulting fees. Timelines can be influenced by the completeness of the application and the FDA’s review process.

Contact Us:

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