Medical Device Manufacturer · US , Waukesha , WI

General Electric Company - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Recent clearances: SENOGRAPHE DS, SENOGRAPHE ESSENTIAL, SENOGRAPH DS, SENOGRAPH ESSENSTIAL

View 2 510(k) Devices ↓ Official Website

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - General Electric Company Radiology ✕

2 devices

1-2 of 2

Cleared Dec 22, 2011

SENOGRAPHE DS, SENOGRAPHE ESSENTIAL

Radiology · 275d

Cleared Oct 06, 2011

SENOGRAPH DS, SENOGRAPH ESSENSTIAL

Radiology · 314d