Sumitomo Heavy Industries, Ltd. is one of 18378 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sumitomo Heavy Industries, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Sumitomo Proton Therapy System, SUMITOMO PROTON THERAPY SYSTEM
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.
510(k) submissions have been managed by Icon Clinical Research, Lcc as regulatory consultant.
FDA 510(k) Regulatory Record - Sumitomo Heavy Industries, Ltd.
2 devices