Skip to content
  • KOSPI 2855.77 +43.72 +1.55%
  • KOSDAQ 764.21 +7.98 +1.06%
  • KOSPI200 382.99 +6.45 +1.72%
  • USD/KRW 1359 14.00 -1.03%
View Market Snapshot
Bio & Pharma

JLK gets OK from FDA for ICH diagnosis solution

It received the FDA's 501K without a completion response letter for its AI-based intracerebral hemorrhage diagnosis solution

By Jan 06, 2025 (Gmt+09:00)

1 Min read

JLK gets OK from FDA for ICH diagnosis solution


South Korea’s JLK Inc., an AI-based diagnosis solution and platform maker, said on Monday it got 501K approval from the US Food and Drug Administration (FDA) for its AI-based intracerebral hemorrhage (ICH) diagnosis solution JLK-ICH.
 
JLK-ICH is an AI solution that analyzes CT images of a patient's brain to detect areas of brain hemorrhage. 

It received the FDA's 501K without a completion response letter (CRL).

JLK explained that this product will work with its existing JLK-LVO, JLK-CTP, and JLK-PWI to address the entire stroke cycle, from diagnosis to treatment decision. 

Write to Jeong Min Nam at peux@hankyung.com

More to Read
Comment 0
0/300