你即將離開本站

並前往https://www.foiservices.com/brochure/devicedocs.cfm

Device Documents - FOI Services

The Center for Devices and Radiological Health (CDRH) within the FDA is responsible ... The PMA undergoes scientific review by appropriate FDA personnel and ...

確定！ 回上一頁

查詢 「510k PMA」的人也找了：

  1. 510k是什麼
    2.
  2. 510k申請
    3.
  3. 510k豁免
    4.
  4. 510k submission
    5.
  5. FDA 510k guidance
    6.
  6. fda 510k費用
    7.
  7. 510k文件
    8.
  8. pma醫材
    9.