Sumitomo Heavy Industries, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sumitomo Heavy Industries, Ltd. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2013 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sumitomo Heavy Industries, Ltd. Filter by specialty or product code using the sidebar.
2 devices