Abbott gets FDA clearance for CGM app
Abbott received FDA clearance for an app to pair with its Freestyle Libre 2 glucose monitor. The app lets people get readings directly on their phone without using a reader.
Abbott received FDA clearance for an app to pair with its Freestyle Libre 2 glucose monitor. The app lets people get readings directly on their phone without using a reader.
Abbott announced the launch of the newly-approved NeuroSphere Virtual Clinic by which deep brain stimulation patients can have their devices programmed and reset remotely, from the comfort of their homes without having to travel to a specialist.
Munck Wilson Mandala Partner Greg Howison shared his perspective on some of the legal ramifications around AI, IP, connected devices and the data they generate, in response to emailed questions.
False negatives increase the risk that patients will not self-isolate or exercise other precautions — such as wearing a mask — and make more people sick than if they had had an accurate diagnosis.
NPR reported on the study by The Cleveland Clinic's Dr. Gary Procop, which has not been peer reviewed. Procop acknowledged that he had stored samples in a special solution not recommended by the company, which defended the ID NOW test.
In a public health crisis such as the Covid-19 pandemic, each healthcare vertical is playing a crucial role. Diagnostics companies are racing to test in the most accurate way possible, biotech and pharma companies are moving mountains to quickly develop vaccines and study potential therapies, while digital health companies have stepped up to the plate […]
The diagnostics company said it had received the EUA for use of its ID NOW system, which can detect a positive result in as low as five minutes and a negative result in 13 minutes. ID NOW is mainly used in urgent care settings.
American pharma companies — architects of the opioid crisis in the United States and avid hunters of new markets — stand at the ready to feed and fuel demand for painkillers in India where attitudes toward pain toleration have changed.
Dexcom's executives lay out the land in terms of competition in the standalone continuous glucose monitoring market while Medtronic CEO responds.
A sooner-than-expected availability of a rival's continuous glucose monitoring system to Medicare patients sends Dexcom's stocks lower, but an analyst believes this will be temporary.
Although DexCom actually was the first to get FDA approval for a continuous glucose monitor with its G5 model last year, it requires finger sticks to calibrate the device.
We will highlight Build My Health's revenue practice management tools, which could help physician practices add up to $250,000 to their practices.
In a new report, the Health Care Council of Chicago, an initiative of Matter and Leavitt Partners, outlined the current status of Chicago's healthcare ecosystem.
Assessing mild traumatic brain injury with a blood test could be tremendously useful for the military. More than 360,000 service members have suffered a TBI since 2000, and diagnosing them has often been inexact
Abbott Vascular's Absorb bioresorbable stent that disappears into the body over time seems to be coming up short compared with the company's durable drug-eluting stent, Xience.
The deal is a win-win for both companies.