Upstream Peripheral Technologies, Ltd. - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.