FDA 510(k) Application Details - K190560

Device Classification Name	Oximeter, Tissue Saturation   More FDA Info for this Device
510(K) Number	K190560
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	Nancy DeAngelo 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	03/05/2019
Decision Date	05/02/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review