LINKÖPING, Sweden, March 27,
2024 /PRNewswire/ -- SyntheticMR announced today that
their next-generation imaging solution with isotropic resolution,
SyMRI 3D, has received FDA 510(k) clearance for clinical use in
the United States.
SyntheticMR is proud to announce that its next-generation
imaging solution, SyMRI 3D, has received FDA 510(k) clearance for
clinical use in the United States.
This milestone marks a significant advancement in quantitative MRI
technology, offering unprecedented resolution and accuracy in brain
imaging.
"We are thrilled to receive 510(k) clearance for SyMRI 3D," says
Ulrik Harrysson, CEO at SyntheticMR AB. "SyMRI 3D represents the
next generation of quantitative MRI, revolutionizing the landscape
of medical diagnostics and offering new possibilities for diagnosis
and treatment."
SyMRI 3D enables precise volumetric estimations of brain
regions, a technique commonly referred to as parcellation, which
empowers clinicians to gain deeper insights into brain structure
and function. Furthermore, the resolution provided by SyMRI 3D
facilitates comprehensive lesion analysis, ensuring a more accurate
and in-depth assessment of medical conditions.
"Receiving 510(k) clearance for SyMRI 3D allows us to empower
physicians to make more precise and informed decisions in diagnosis
and treatment planning through quantitative imaging," says
Jared Dixon, President of
SyntheticMR U.S Inc.
With this clearance, SyntheticMR reaffirms its commitment to
advancing medical imaging technology and providing clinicians with
innovative tools to enhance patient care. SyMRI 3D opens up new
possibilities for precise diagnosis, treatment planning, and
monitoring, ultimately improving patient outcomes.
This disclosure contains information that SyntheticMR AB is
obliged to make public pursuant to the EU Market Abuse Regulation
(EU nr 596/2014). The information was submitted for publication,
through the agency of the contact person, on 27-03-2024 11:01
CET.
For additional information, please contact Ulrik Harrysson, CEO,
SyntheticMR AB, +46 70 529 29 87 ulrik.harrysson@syntheticmr.com or
Jared Dixon, President SyntheticMR
U.S Inc. at +1 (859) 2401965 or jared.dixon@syntheticmr.com
This information was brought to you by Cision
http://news.cision.com
https://news.cision.com/syntheticmr-ab/r/syntheticmr-receives-fda-510-k--clearance-for-their-next-generation-solution-symri-3d,c3953367
The following files are available for download:
https://mb.cision.com/Main/11663/3953367/2700237.pdf
|
SyntheticMR receives
FDA 510(k) clearance
|
View original
content:https://www.prnewswire.com/news-releases/syntheticmr-receives-fda-510k-clearance-for-their-next-generation-solution-symri-3d-302100919.html
SOURCE SyntheticMR AB