FDA 510(k) Application Details - K022819

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K022819
Device Name	Oximeter
Applicant	NELLCOR PURITAN BENNETT, INC. 4280 HACIENDA DR. PLEASANTON, CA 94588-2719 US Other 510(k) Applications for this Company
Contact	GINA TO 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	08/26/2002
Decision Date	09/24/2002
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