Technology | Digital Radiography (DR) | February 20, 2019

Philips Earns FDA Clearance for DigitalDiagnost C90 DR System

Premium ceiling-mounted system supports accelerated patient throughput with tools like a live camera image at the tube head that help produce high-quality images and drive workflow efficiency

Philips Earns FDA Clearance for DigitalDiagnost C90 DR System

February 20, 2019 — Philips announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the DigitalDiagnost C90, its newest premium digital radiography (DR) system. Designed to increase patient throughput and decrease the time to diagnosis, the Philips DigitalDiagnost C90 offers healthcare organizations a flexible and customizable imaging solution that helps to improve workflow and clinical outcomes, while adding economic value.

X-ray is often the start of a patient’s care journey and plays a critical role in supporting clinical care decisions from that point forward, making high-quality imaging essential. As the industry’s first radiography unit with a live camera image directly displayed at the tube head, DigitalDiagnost provides a clear view of the anatomical area being scanned during the patient positioning process – improving workflow so that clinicians can be confident that the right area is captured with a low X-ray dose exposure. With Philips’ UNIQUE 2 image processing and Riverain Technologies’ ClearRead Bone Suppression software, radiologists can process clearer images for a more confident diagnosis with a lower chance of a costly and timely rescan.

The system also incorporates the Philips Eleva user interface, a common platform across a range of Philips DR systems that enables a smooth and efficient patient-focused workflow. This common user interface is now extended to the Eleva Tube Head, speeding up workflow by more than 17 percent per examination [1]. Its touch-screen display transfers operation into the examination room to allow for more time with the patient. DigitalDiagnost also helps contribute to a lower cost of care, with flexible room configuration options and SkyPlate sharing available among all Philips premium digital radiography systems.

For more information: www.usa.philips.com/healthcare

References

[1] Compared to a typical examination using the previous release of Philips’ DigitalDiagnost. Based on four images on average per examination. Validated by clinicians in a Philips development environment.

Related Content

Fujifilm Sonosite Partnering With Artificial Intelligence Incubator to Improve Ultrasound Image Interpretation
News | Ultrasound Imaging | September 23, 2019
Fujifilm SonoSite Inc. and the Allen Institute of Artificial Intelligence (AI2) Incubator, builder of AI-first startups...
Densitas Wins Major Procurement of Breast Density Software for DIMASOS Breast Screening Trial
News | Breast Density | September 20, 2019
Densitas Inc. announced it has won a procurement of its densitas densityai software for deployment in up to 24 breast...
Screening Mammography Could Benefit Men at High Risk of Breast Cancer
News | Mammography | September 18, 2019
Selective mammography screening can provide potentially lifesaving early detection of breast cancer in men who are at...
Nurse Practitioners, Physician Assistants Rarely Interpret Diagnostic Imaging Studies
News | Radiology Business | September 18, 2019
September 18, 2019 — Although Medicare claims data confirm the...
The Artis icono biplane angiography system is designed for use in neurointerventions and interventional radiology

The Artis icono biplane angiography system is designed for use in neurointerventions and interventional radiology. Image courtesy of Siemens Healthineers.

Technology | Angiography | September 17, 2019
The U.S. Food and Drug Administration (FDA) has cleared the Artis icono, a high-precision family of angiography systems...
3D Systems Earns Additional FDA Clearance for D2P Medical 3-D Printing Software

3D Systems’ D2P FDA-cleared software allows clinicians to 3-D-print diagnostic patient-specific anatomic models. Image courtesy of 3D Systems.

Technology | Medical 3-D Printing | September 12, 2019
3D Systems has received additional U.S. Food and Drug Administration (FDA) 510(k) clearance for its D2P software...
FDA Clears GE Healthcare's Critical Care Suite Chest X-ray AI
Technology | X-Ray | September 12, 2019
GE Healthcare announced the U.S. Food and Drug Administration’s (FDA) 510(k) clearance of Critical Care Suite, a...
Richardson Healthcare Receives CE Mark Approval for ALTA750 Canon/Toshiba CT Replacement Tube
News | Computed Tomography (CT) | September 11, 2019
Richardson Healthcare, a Division of Richardson Electronics Ltd., announced it has received CE Mark approval for the...
Bayer Introduces Medrad Stellant Flex CT Injection System
Technology | Contrast Media Injectors | September 11, 2019
Bayer announced the introduction of the Medrad Stellant Flex computed tomography (CT) injection system. Stellant Flex...
iCAD's ProFound AI Wins Best New Radiology Solution in 2019 MedTech Breakthrough Awards
News | Computer-Aided Detection Software | September 09, 2019
iCAD Inc. announced MedTech Breakthrough, an independent organization that recognizes the top companies and solutions...