FDA 510(k) Application Details - K030668

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K030668
Device Name	Oximeter
Applicant	NONIN MEDICAL, INC. 2605 FERNBROOK LANE, NORTH MINNEAPOLIS, MN 55447-4755 US Other 510(k) Applications for this Company
Contact	RICHARD P BENNETT 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	03/03/2003
Decision Date	10/17/2003
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