FDA 510(k) Application Details - K243420

Device Classification Name	Full Field Digital,System,X-Ray,Mammographic   More FDA Info for this Device
510(K) Number	K243420
Device Name	Full Field Digital,System,X-Ray,Mammographic
Applicant	GENORAY Co., Ltd. 60, Dunchon-daero 541beon-gil Jungwon-gu Seongnam-si 13212 KR Other 510(k) Applications for this Company
Contact	Jiyeon Choi Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MUE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/04/2024
Decision Date	07/17/2025
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