FDA 510(k) Application Details - K071610

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K071610
Device Name	Oximeter
Applicant	MEDIAID INC. 17517 FABRICA WAY, SUITE H CERRITOS, CA 90703 US Other 510(k) Applications for this Company
Contact	JAYESH PATEL 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	06/13/2007
Decision Date	11/05/2007
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