FDA 510(k) Application Details - K040917

Device Classification Name	Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)   More FDA Info for this Device
510(K) Number	K040917
Device Name	Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)
Applicant	PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 BOEBLINGEN D 71034 DE Other 510(k) Applications for this Company
Contact	HERBERT VAN DYK Other 510(k) Applications for this Contact
Regulation Number	868.1500   More FDA Info for this Regulation Number
Classification Product Code	CBQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/08/2004
Decision Date	04/29/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review