Edda Technology, Inc. is one of 19001 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Edda Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IQQA-LIVER MULTIMODALITY SOFTWARE, IQQA-LIVER SOFTWARE, IQQA-CHEST SOFTWARE PACKAGE
3
Total
3
Cleared
0
Denied
Edda Technology, Inc. has 3 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 3 cleared submissions from 2004 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Edda Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Edda Technology, Inc.
3 devices