FDA 510(k) Application Details - K073407

Device Classification Name	Oximeter, Tissue Saturation   More FDA Info for this Device
510(K) Number	K073407
Device Name	Oximeter, Tissue Saturation
Applicant	OR-NIM MEDICAL LTD. 2001 PENNSYLVANIA AVE. NW SUITE 950 WASHINGTON, DC 20006 US Other 510(k) Applications for this Company
Contact	CAMPBELL HUTTON 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	12/04/2007
Decision Date	02/28/2008
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