Medical Device Manufacturer · US , Laurel , MD

Ge Healthcare Clinical Systems - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007
1
Total
1
Cleared
0
Denied

Ge Healthcare Clinical Systems has 1 FDA 510(k) cleared medical devices. Based in Laurel, US.

Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Ge Healthcare Clinical Systems Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ge Healthcare Clinical Systems

1 devices
1-1 of 1
Filters
All1 General Hospital 1