FDA 510(k) Application Details - K151305

Device Classification Name	Oximeter, Tissue Saturation   More FDA Info for this Device
510(K) Number	K151305
Device Name	Oximeter, Tissue Saturation
Applicant	NONIN MEDICAL INC. 13700 1ST AVENUE NORTH PLYMOUTH, MN 55441 US Other 510(k) Applications for this Company
Contact	LAURA J. LIND Other 510(k) Applications for this Contact
Regulation Number	870.2700   More FDA Info for this Regulation Number
Classification Product Code	MUD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/18/2015
Decision Date	08/27/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review