FDA 510(k) Application Details - K131111

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K131111
Device Name	Oximeter
Applicant	ANDON HEALTH CO.,LTD #3, JIN PING STREET YA AN RD NANKAI DISTRICT TIANJIN 300190 CN Other 510(k) Applications for this Company
Contact	LIU Yi 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	04/19/2013
Decision Date	09/11/2013
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