FDA 510(k) Application Details - K231660

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K231660
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	Jiangsu Dynamic Medical Technology Co., Ltd. No. 108 Xingpu Road, Lujia Town, Kunshan Suzhou 215331 CN Other 510(k) Applications for this Company
Contact	Xiang Long Liu 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	06/07/2023
Decision Date	12/20/2023
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