The FDA has released its report “FDA Report on the Quality, Safety, and Effectiveness of Servicing of Medical Devices in accordance with Section 710 of the Food and Drug Administration Reauthorization Act of 2017 (FDARA).”
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CurveBeam announced it has received FDA 510(k) clearance for its LineUP Multi-extremity weight bearing CT system.
This 60-minute webinar provided an overview of X-ray quality assurance by looking at how technology has driven efficiency over the past 20 years.
Greene cited Carestream’s service record as an important benefit to investing in the company’s imaging systems.
The Dynamic Cardiac Phantom “is a precision instrument that simulates the realistic motion of an average human heart.
Global Medical Imaging (GMI), soon to be Avante Ultrasound, has received its certificate of registration to the Medical Devices Quality Management Standard of ISO 13485:2016.
The InterMed Group has announced the acquisition of Medical Imaging Technologies Inc. (M.I.T.).
The voluntary, consensus-based NEMA Standard will outline the minimum quality management system requirements for medical device servicing.
A research team discovered a way to turn plain old H20 into a very effective contrast agent used in magnetic resonance imaging, or MRI.
Kubtec will be introducing new innovations designed to enhance and improve the surgical treatment of breast cancer at the annual meeting of the American Society of Breast Surgeons in Orlando.
