Applied Diabetes Research, Incorporated is one of 25799 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Diabetes Research, Incorporated - FDA 510(k) Cleared Devices
Recent clearances: ADR THINSET INFUSION SET MODEL, 23-106, 23-109, 43-106, 43-109, SURESET 3.0 ML RESERVOIR, MODEL 24-103, SURESET INFUSION SET, MODEL 8023
3
Total
3
Cleared
0
Denied
Applied Diabetes Research, Incorporated has 3 FDA 510(k) cleared medical devices. Based in Chapel Hill, US.
Historical record: 3 cleared submissions from 2001 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Applied Diabetes Research, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Applied Diabetes Research, Incorporated
3 devices