FDA 510(k) Application Details - K230581

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K230581
Device Name	System, X-Ray, Mobile
Applicant	NEUF Inc. #103 Production Bldg. 13, Yulchonsandan 4-ro, Haeryong-myeon Suncheon-si 58034 KR Other 510(k) Applications for this Company
Contact	Woo Sang Lee Other 510(k) Applications for this Contact
Regulation Number	892.1720   More FDA Info for this Regulation Number
Classification Product Code	IZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/02/2023
Decision Date	08/16/2023
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