Medical Device Manufacturer · US , New Haven , CT

Ikonisys, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2006

Total

Cleared

Denied

Ikonisys, Inc. has 4 FDA 510(k) cleared medical devices. Based in New Haven, US.

Historical record: 4 cleared submissions from 2006 to 2008. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Ikonisys, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ikonisys, Inc.

4 devices

1-4 of 4