Soma Access Systems LLC received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its AxoTrack sterile procedure kit. Portable ultrasound maker Terason also recently received 510(k) clearance for the first ultrasound probe to be equipped with Soma’s patented AxoTrack virtual needle technology.

March 29, 2012 — Siemens Healthcare recently expanded its solutions portfolio by offering the RaySafe i2 personal dosimetry system as an accessory for all Siemens Artis zee angiography systems. By using RaySafe i2 during imaging procedures, medical personnel obtain real-time information regarding their levels of radiation exposure, enabling them to take immediate steps to minimize exposure and establish a high-functioning radiation safety culture within their hospital.

March 28, 2012 - Accuray Incorporated, a radiation oncology company, announced the release of PlanTouch, the first commercially available, fully integrated software application in radiation oncology that allows physicians to remotely review and approve patients' radiation treatment plans on the iPad. The PlanTouch software, developed in partnership with MIM Software Inc., frees physicians using the CyberKnife Robotic Radiosurgery System from work stations and provides them with increased collaboration, mobility, flexibility and convenience in delivering high-quality patient care. PlanTouch has received 510(k) clearance from the U.S. Food & Drug Administration (FDA).

GE Healthcare unveiled two recently U.S. Food and Drug Administration (FDA)-cleared angiography systems offering mobility and advanced imaging for interventional cardiology at the American College of Cardiology (ACC) 2012.