FDA 510(k) Application Details - K232325

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K232325
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	Ray Co., Ltd. 1F-3F, 4F(Part), 5F, 265, Daeji-Ro, Suji-gu Yongin-si 16882 KR Other 510(k) Applications for this Company
Contact	Sooji Huh Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	MUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/03/2023
Decision Date	04/18/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review