Medscape

Panel Agrees Spinal Sphere Devices Need Premarket Approval

Given the lack of information on their effectiveness and the unreasonable risks for illness or injury, spinal sphere devices should be regulated as Class 3 devices that require premarket approval (PMA ...
techtimes

Google Home Panel for Pixel Devices Now Available: Users can Quickly Access Their Home Devices

The Google Home app is getting an update with a home panel that allows users to better monitor home devices. This comes after Google announced the public rollout of the revamped version of its app.
STAT

FDA panel asks for improvements in pulse oximeters

A Food and Drug Administration advisory panel suggested Tuesday that the agency improve how it regulates pulse oximeters, calling for clearer labeling and more rigorous testing of the devices. The ...

I transformed my Windows 11 start menu into an Android app drawer - here's how

Microsoft's redesigned Windows 11 Start Menu is a step-up over its predecessor, squarely because I can turn it into an ...
Chicago Sun-Times

FDA panel reviewing Abbott heart device included 10 doctors with financial ties to the north suburban health giant

Why are we asking for donations? Why are we asking for donations? This site is free thanks to our community of supporters. Voluntary donations from readers like you keep our news accessible for ...
MedPage Today

FDA Panel Mulls Which Devices Are Critical in a Public Health Emergency

Share on Facebook. Opens in a new tab or window Share on Bluesky. Opens in a new tab or window Share on X. Opens in a new tab or window Share on LinkedIn. Opens in a new tab or window What bare ...
Healio

FDA panel says risks of radiofrequency renal denervation device outweigh benefits

Please provide your email address to receive an email when new articles are posted on . An FDA panel voted that for adults with uncontrolled hypertension, the benefits of a radiofrequency renal ...
AOL

US FDA panel votes against use of Medtronic's blood pressure treatment device

(Reuters) -The U.S. Food and Drug Administration's (FDA) independent experts on Wednesday narrowly voted against recommending the approval of Medtronic's blood pressure treatment device, saying risks ...
2UrbanGirls on MSN

Smart electrical panel features that actually deliver usable energy insights

As we move deeper into 2026, the humble breaker box is no longer just a passive safety device tucked away in the garage. The ...
Star Tribune

Medtronic hypertension device faces new challenges after FDA advisory panel vote

Medtronic suffered a regulatory and competitive setback Wednesday after a U.S. Food and Drug Administration advisory panel expressed concerns about Symplicity Spyral, a device to treat hypertension.
MedPage Today

FDA Panel Backs Cryoablation in Early Breast Cancer as Alternative to Surgery

An FDA panel on Thursday endorsed a cryoablation system as an alternative to surgery for some early breast cancer patients. By a 9-5 vote, the General and Plastic Surgery Devices Panel of the Medical ...