'iSyncWave' EEG Scanner receives FDA 510k clearance

SEOUL,South Korea,Sept. 23,2022 -- iMediSync announced that iSyncWave,the company's medical device EEG scanner,hasbeen granted 510k clearance from the US Food and Drug Administration (FDA) on August 10th.

iMediSync’s EEG scanner ‘iSyncWave’ has been FDA 510k cleared

According to iMediSync,iSyncWave is a dry EEG scanner that does not require the use ofelectrode gel. It is not only easy to wear the device and measure EEG,butthe size of the device can also be adjusted to accommodate various head shapes and align with the internationally standardized 10-20 system.Furthermore,iSyncWave analyzesthe QEEG (Quantitative Electroencephalogram) in a short periodof time through big data based automatic cloud analysis system.

This devicewas recently registered as an innovative prototype product by the Public Procurement Service in South Korea and was introduced to the mobile medical checkup service at Pusan National University Hospital.Data is continuouslycollected from patientswith various diseasesand illnesses (stroke,Parkinson's,etc.)at leading university hospitals in South Korea,such as Seoul National University Hospital and Asan Medical Center.

In September,iSyncWave will be presentedat the University of Oxford EEG seminar for children with developmental disabilities.

Following the FDA 510k clearance,iMediSync plans to increase and expand overseas sales.

Seungwan Kang,the CEO of iMediSyncstated,"After CES 2022and AAIC (Alzheimer's Association International Conference),we arereceiving many inquiries from the US,Europe,Australia,and other countries,particularly aroundresearch and clinical introduction from leading universities and institutions around the world. With FDA 510k clearance,we can provide product information and conduct collaborative research to sell iSyncWave. We are also preparing the CE (EU),TGA (Australia) and PMDA (Japan) registrations for countries that require registration other than from the FDA for import."

Homepage:https://www.imedisync.com/en/

View original content to download multimedia:https://www.prnewswire.com/news-releases/isyncwave-eeg-scanner-receives-fda-510k-clearance-301631945.html