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