FDA 510(k) Application Details - K062268

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K062268
Device Name	Oximeter
Applicant	PHILIPS MEDICAL SYSTEMS NORTH AMERICA CO. 3000 MINUTEMAN ROAD ANDOVER, MA 01810-1099 US Other 510(k) Applications for this Company
Contact	DAVID OSBORN 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	08/07/2006
Decision Date	10/18/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review