Mevis Technology GmbH & Co. KG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mevis Technology GmbH & Co. KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mevis Technology GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mevis Technology GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mevis Technology GmbH & Co. KG
1 devices