Medical Device Manufacturer · FI , Helsinki

Ge Healthcare Filand OY - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2015

Recent clearances: Entropy Module, E-ENTROPY-01

1
Total
1
Cleared
0
Denied

Ge Healthcare Filand OY has 1 FDA 510(k) cleared medical devices. Based in Helsinki, FI.

Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.

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

510(k) submissions have been managed by GE Healthcare as regulatory consultant.

FDA 510(k) Regulatory Record - Ge Healthcare Filand OY

1 devices
1-1 of 1
Filters
All1 Neurology 1