Duopross Meditech Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Duopross Meditech Corporation - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Duopross Meditech Corporation has 2 FDA 510(k) cleared medical devices. Based in Albuquerque, US.
Historical record: 2 cleared submissions from 2005 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Duopross Meditech Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Duopross Meditech Corporation
2 devices