FDA 510(k) Application Details - K070371

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K070371
Device Name	Oximeter
Applicant	BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD. SUITE 8D ZHONGXIN ZHONGSHAN MANSION, NO. 19 LANE, 999 SHANGHAI, SHANGHAI 20020 CN Other 510(k) Applications for this Company
Contact	Diana Hong Other 510(k) Applications for this Contact
Regulation Number	870.2700   More FDA Info for this Regulation Number
Classification Product Code	DQA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/08/2007
Decision Date	08/13/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review