Medical Device Manufacturer · US , Urbandale , IA

Scandia Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010
1
Total
1
Cleared
0
Denied

Scandia Corporation has 1 FDA 510(k) cleared medical devices. Based in Urbandale, US.

Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Scandia Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Scandia Corporation
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