DEKA Research & Development is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
DEKA Research & Development - FDA 510(k) Cleared Devices
Recent clearances: Unity Subcutaneous Infusion System for Remodulin, Unity Subcutaneous Delivery System for Remodulin
3
Total
3
Cleared
0
Denied
DEKA Research & Development has 3 FDA 510(k) cleared medical devices. Based in Manchester, US.
Historical record: 3 cleared submissions from 2016 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by DEKA Research & Development Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - DEKA Research & Development
3 devices