'''''Following a recent warning from the US Food and Drug Administration (FDA) on the safety of certain ultrasound contrast agents (UCAs) containing polyethylene glycol (PEG), the American Institute of Ultrasound in Medicine (AIUM) joins the International ...'

'''''The U.S. Food and Drug Administration (FDA) cleared software to assist medical professionals in the acquisition of cardiac ultrasound, or echocardiography, images. The software, called Caption Guidance, is an accessory to compatible diagnostic ultrasound ...'

'''''Analogic Corp. (ALOG: Quote) announced that it has received 510(k) clearance from the U.S. Food and Drug Administration or FDA for the handheld Sonic Window ultrasound system, an imaging device for visualizing vasculature and guiding peripheral ...'

'''''InSightec Image Guided Treatment Ltd. has obtained US Food and Drug Administration (FDA) premarketing approval for the company's ExAblate targeted focused ultrasound treatment for the removal of bone tumors. The approval is initially for patients who ...'

'''''Echometrix, a Madison medical technology company, has received U.S. Food and Drug Administration approval to sell its EchoSoft ultrasound technology. We're very pleased to have reached this critical milestone, said chief executive Sam Adams. The ...'

'''''On August 20, 2012, InSightec announced it received approval from the Food and Drug Administration (FDA) to begin Phase I clinical trials evaluating the use of its ExAblate Neuro system for the treatment of patients with tremor-dominant Parkinson’s ...'

'''''Acusphere, Inc. (ACUS.PK), a specialty pharmaceutical company, today announced that it had reached an agreement with the U.S. Food & Drug Administration (FDA) regarding the design of a new Phase 3 study of the company’s lead product candidate, Imagify™ ...'

'''''A steady procession of mobile health devices continues to march through the FDA’s regulatory process. The US Food and Drug Administration has granted Redmond, Washington-based mobile health start-up Mobisante 510(k) clearance for its smartphone-based ...'

'''''US HIFU has expanded with a $5.8 million technology acquisition. The move gives the Charlotte medical-device company its first U.S. Food and Drug Administration-approved device in the Sonatherm 600. That laparoscopic tool uses high-intensity focused ...'

'''''A Mesa medical device maker has received approval from the U.S. Food and Drug Administration to begin marketing its ultrasound technology to perform eyebrow lifts without surgery. Next, it hopes the same technology will be OK’d for other applications ...'