FDA 510(k) Application Details - K151854

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K151854
Device Name	System, Image Processing, Radiological
Applicant	D-VIEW DISPLAY TECHNOLOGY CO., LTD. 3F, BUILDING 4, NO.12# KECHUANG 13TH STREET, BDA AREA BEI JING 100176 CN Other 510(k) Applications for this Company
Contact	JIANFEI SUN Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/07/2015
Decision Date	07/28/2015
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