D4D Technologies is one of 24587 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
D4D Technologies - FDA 510(k) Cleared Devices
Recent clearances: E4D COMPASS
1
Total
1
Cleared
0
Denied
D4D Technologies has 1 FDA 510(k) cleared medical devices. Based in Carmel, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by D4D Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - D4D Technologies
1 devices