Medical Device Manufacturer · US , Gainesvilles , FL

The R Group - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1991
4
Total
4
Cleared
0
Denied

The R Group has 4 FDA 510(k) cleared medical devices. Based in Gainesvilles, US.

Historical record: 4 cleared submissions from 1991 to 1991. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - The R Group

4 devices
1-4 of 4
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