FDA 510(k) Application Details - K082268

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K082268
Device Name	Oximeter
Applicant	ORIDION CAPNOGRAPHY, INC. HAR HOTZVIM SCIENCE PARK POB 45025 JERUSALEM 91450 IL Other 510(k) Applications for this Company
Contact	RACHEL WEISSBROD 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	08/11/2008
Decision Date	02/06/2009
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