FDA Clears YorLabs Intracardiac Imaging System
The no-capital-expenditure ultrasound platform is designed to simplify workflow, reduce cost, and enhance procedural efficiency inside the cath lab.
The no-capital-expenditure ultrasound platform is designed to simplify workflow, reduce cost, and enhance procedural efficiency inside the cath lab.
The system is cleared to produce tomographic images for general use, including musculoskeletal, pulmonary, intra-abdominal, and paranasal indications.
Tahoe Forest Health System is the first U.S. facility to install Siemens Healthineers' Ciartic Move mobile C-arm.
The no-capital-expenditure ultrasound platform is designed to simplify workflow, reduce cost, and enhance procedural efficiency inside the cath lab.
Powering down idle-running interventional imaging systems outside of procedure times has substantial environmental sustainability benefits, according to new research.
Read MorePhilips has recalled its BrightView SPECT imaging systems for a potential component failure that would cause parts to fall on the patient.
Read MoreGE HealthCare announced FDA 510(k) clearance of Allia IGS Pulse – the latest addition to the company’s image guided system (IGS) offerings.
Read MoreGE HealthCare has launched Vscan Air SL, a handheld wireless ultrasound system designed for quick cardiac and vascular assessments at the point of care.
Read MoreFujifilm Healthcare Americas announced FDA 510(k) clearance of its new 1.5 Tesla MRI system, the Echelon Synergy.Â
Read MorePentax Medical America obtained US FDA 510(k) clearance for the Pentax Medical Inspira 4K video processor and the i20c video endoscope series.
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Imeka announced that the FDA has granted 510(k) clearance for its Advanced Neuro Diagnostic Imaging (ANDI) quantitative imaging software.