Upstream Peripheral Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Upstream Peripheral Technologies - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Upstream Peripheral Technologies has 3 FDA 510(k) cleared medical devices. Based in Philedelphia, US.
Historical record: 3 cleared submissions from 2012 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Upstream Peripheral Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Upstream Peripheral Technologies
3 devices