Medical Device Manufacturer · US , Mountainside , NJ

D.R.G. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985

Total

Cleared

Denied

D.R.G. has 2 FDA 510(k) cleared medical devices. Based in Mountainside, US.

Historical record: 2 cleared submissions from 1985 to 1989. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - D.R.G.

2 devices

1-2 of 2