Deka Research and Development Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deka Research and Development Corporation - FDA 510(k) Cleared Devices
Recent clearances: DEKA Infusion System, DEKA Administration Set
1
Total
1
Cleared
0
Denied
Deka Research and Development Corporation has 1 FDA 510(k) cleared medical devices. Based in Manchester, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Deka Research and Development Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Deka Research and Development Corporation
1 devices