Gentec (Shanghai) Corporation is one of 2135 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Gentec (Shanghai) Corporation - FDA 510(k) Cleared Devices
Recent clearances: GMX Series Medical Air/Oxygen Blender
1
Total
1
Cleared
0
Denied
Gentec (Shanghai) Corporation has 1 FDA 510(k) cleared medical devices. Based in Songjiang District, CN.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Gentec (Shanghai) Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Guangzhou Osmunda Medical Device Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Gentec (Shanghai) Corporation
1 devices