FDA 510(k) Application Details - K982969

Device Classification Name	Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase   More FDA Info for this Device
510(K) Number	K982969
Device Name	Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
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	868.1400   More FDA Info for this Regulation Number
Classification Product Code	CCK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/25/1998
Decision Date	08/12/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review