Medical Device Manufacturer · US , Dublin , CA

Sonoscape Company Limited - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 2004
22
Total
22
Cleared
0
Denied

Sonoscape Company Limited has 22 FDA 510(k) cleared radiology devices. Based in Dublin, US.

Historical record: 22 cleared submissions from 2004 to 2015.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sonoscape Company Limited
22 devices
1-12 of 22
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