Renalpro Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renalpro Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AortaSTAT Occlusion Device
1
Total
1
Cleared
0
Denied
Renalpro Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Renalpro Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Northwest Clinical Research Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Renalpro Medical, Inc.
1 devices