FDA clears GE's patient-assisted compression mammo unit
The U.S. Food and Drug Administration (FDA) has cleared GE Healthcare's Senographe...Read more on AuntMinnie.comRelated Reading:
GE signs cyclotron partnership with Canadian firm
GE gets FDA nod for new Signa Premier MRI
GE names new CEO for India, South Asia
GE Healthcare buys consulting firm
GE installs 1st 3D DBT Senographe Pristina in U.S.
Source: AuntMinnie.com Headlines - Category: Radiology Source Type: news