Medical Device Manufacturer · US , Minneapolis , MN

Rand S.R.L. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2006

Total

Cleared

Denied

Rand S.R.L. has 4 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 4 cleared submissions from 2006 to 2016. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Rand S.R.L. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Rand S.R.L.

4 devices

1-4 of 4