This site uses cookies to improve your experience. To help us insure we adhere to various privacy regulations, please select your country/region of residence. If you do not select a country, we will assume you are from the United States. Select your Cookie Settings or view our Privacy Policy and Terms of Use.
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Used for the proper function of the website
Used for monitoring website traffic and interactions
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Strictly Necessary: Used for the proper function of the website
Performance/Analytics: Used for monitoring website traffic and interactions
Powered by artificial intelligence (AI), the Rapid NCCT Stroke modality is reportedly the first medicaldevice to gain FDA 510(k) clearance for detecting suspected large vessel occlusion and intracranial hemorrhage based on assessment of non-contrast computedtomography (NCCT).
French imaging software developer Median Technologies has secured nearly $50 million to support regulatory filings for its AI lung cancer diagnostic software as a medicaldevice (SaMD). Several financial decisions have extended the company's cash runway for this year, including a European Investment Bank (EIB) loan for 37.5
announced its latest configuration of the mobile computedtomography (CT) OmniTom Elite with Photon Counting Detector (PCD) technology has received U.S. We will continue to develop leading technologies to improve medical staff's convenience and diagnostic accuracy. Food and Drug Administration (FDA) 510(k) clearance.
announced its latest configuration of the mobile computedtomography (CT) OmniTom Elite with Photon Counting Detector (PCD) technology has received U.S. We will continue to develop leading technologies to improve medical staff's convenience and diagnostic accuracy. Food and Drug Administration ( FDA ) 510(k) clearance.
milla1cf Fri, 06/14/2024 - 19:17 June 14, 2024 — Positron Corporation , a leading molecular imaging medicaldevice company offering PET and PET-CT (Positron Emission Tomography/ComputedTomography) imaging systems and clinical services, announced its membership in the national alliance “Cardiac PET Industry Coalition” (CPIC), an organization at the (..)
AI’s use in radiology continues to grow as the technology becomes more available, according to a presentation given September 12 at the International Society for ComputedTomography (ISCT) annual meeting in Boston. The number of AI-based medicaldevices cleared by the U.S.
milla1cf Tue, 06/18/2024 - 20:02 June 18, 2024 — Positron Corporation , a leading molecular imaging medicaldevice company offering PET and PET-CT (Positron Emission Tomography/ComputedTomography) imaging systems and clinical services, is pleased to welcome a prominent cardiovascular practice in Michigan as a new customer utilizing Positron’s Attrius (..)
milla1cf Thu, 06/13/2024 - 20:46 June 13, 2024 — Positron Corporation , a leading molecular imaging medicaldevice company offering PET and PET-CT (Positron Emission Tomography/ComputedTomography) imaging systems and clinical support services, announced it has entered an agreement to acquire the FDA 510(k) for the NeuSight PET-CT from its cooperative (..)
The software enables users to connect to computedtomography (CT), magnetic resonance (MR), positron emission tomography (PET), single-photon emission CT (SPECT), PET/CT , SPECT/CT, and PET/MR scanners from Siemens Healthineers as well as other equipment vendors, regardless of location.
CT-Navigation – which includes a mobile workstation, guidance software, and disposable procedure kit – is approved under the European Union’s MedicalDevices Regulation (MDR) and has FDA clearance for use within the U.S.
Making MRIs safer for these patients is something medicaldevice makers, the medical community at large, and our radiologists have strived to address. However, in recent years advances in knowledge and the design of pacemaker devices provide additional protection.
.: 553 Date Initiated by Firm: December 15, 2023 Device Use The Philips Brightview system is a Single Photon Emission ComputedTomography ( SPECT ) machine used to take images showing biological activity in the human body, for medical personnel to review. Contact Information Customers in the U.S.
We organize all of the trending information in your field so you don't have to. Join 5,000 users and stay up to date on the latest articles your peers are reading.
You know about us, now we want to get to know you!
Let's personalize your content
Let's get even more personalized
We recognize your account from another site in our network, please click 'Send Email' below to continue with verifying your account and setting a password.
Let's personalize your content