FDA 510(k) Application Details - K233457

Device Classification Name	More FDA Info for this Device
510(K) Number	K233457
Device Name	RUS
Applicant	Hutom Inc. 6F, 279, Dongmak-ro, Mapo-gu Seoul 04151 KR Other 510(k) Applications for this Company
Contact	Heejoo Yun Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/20/2023
Decision Date	07/12/2024
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