Polarean’s FDA cleared coil achieves important milestone, expanding clinical reach XENOVIEW® 3T coil passes Philips ...

Polarean Imaging (PLLWF) has received 510(k) clearance from the U.S. Food and Drug Administration for the Company’s specialized MRI Chest Coil to now include GE HealthCare (GEHC) 3 Tesla MRI scanners ...

Philips has introduced the helium-free 3.0T magnetic resonance imaging (MRI) innovation platform, BlueSeal Horizon.

GE HealthCare (Nasdaq: GEHC) announced that it submitted its next-generation Signa Bolt MRI technology to the FDA for 510(k) ...

GE HealthCare GEHC recently unveiled its next-generation SIGNA MRI portfolio, the 3T SIGNA Bolt and 1.5T SIGNA Sprint with ...

Provider mix and costs associated with treatment of patients with bone metastases secondary to prostate cancer. This is an ASCO Meeting Abstract from the 2012 ASCO Annual Meeting I. This abstract does ...

IMRIS has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the new InVision 3T Recharge Operating Suite We’re delighted to be able to offer our IMRIS customers currently ...

CINCINNATI--(BUSINESS WIRE)--Eyas Medical Imaging is proud to announce the first installation of the groundbreaking neonatal Magnetic Resonance Imaging (MRI) system, the Ascent 3T™, within the ...

Polarean Imaging (PLLWF) announces that its FDA-cleared XENOVIEW 3T Chest Coil has completed compatibility testing conducted by Philips and is now ...