FDA 510(k) Application Details - K242019

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K242019
Device Name	System, X-Ray, Stationary
Applicant	DRGEM Corporation 7F, E-B/D Gwangmyeong Techno-Park, 60Haan-ro, GwangMyeong-si 14322 KR Other 510(k) Applications for this Company
Contact	Jongseon Park Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/10/2024
Decision Date	01/07/2025
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