Medical Device Manufacturer · US , Santa Clara , CA

Renalpro Medical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
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
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