Upstream Peripheral Technologies, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Upstream Peripheral Technologies, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Caesarea, IL.
Last cleared in 2022. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Upstream Peripheral Technologies, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Upstream Peripheral Technologies, Ltd.
2 devices