FDA 510(k) Application Details - K081601

Device Classification Name	Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase   More FDA Info for this Device
510(K) Number	K081601
Device Name	Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Applicant	PHASEIN AB 4213 WINNEQUAH DR. MADISON, WI 53716 US Other 510(k) Applications for this Company
Contact	DAVID WEISSBURG 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	06/06/2008
Decision Date	09/04/2008
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