Medical Device Manufacturer · US , Chester , NY

Ascendia Medtech AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005
1
Total
1
Cleared
0
Denied

Ascendia Medtech AB has 1 FDA 510(k) cleared medical devices. Based in Chester, US.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Ascendia Medtech AB Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ascendia Medtech AB
1 devices
1-1 of 1
Filters
All1 Radiology 1