FDA 510(k) Application Details - K240291

Device Classification Name	More FDA Info for this Device
510(K) Number	K240291
Device Name	EFAI CARDIOSUITE CTA ACUTE AORTIC SYNDROME ASSESSMENT SYSTEM
Applicant	Ever Fortune.AI, Co., Ltd. Rm. D, 8F. No. 573, Sec. 2 Taiwan Blvd. West Dist. Taichung City 403020 TW Other 510(k) Applications for this Company
Contact	Joseph Chang Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QAS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/01/2024
Decision Date	04/08/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review