FDA 510(k) Application Details - K051666

Device Classification Name	Vaporizer, Anesthesia, Non-Heated   More FDA Info for this Device
510(K) Number	K051666
Device Name	Vaporizer, Anesthesia, Non-Heated
Applicant	GENERAL ANAESTHETIC SERVICES LIMITED INGROW BRIDGE BUSINESS PARK HALIFAX ROAD KEIGHLEY, WEST YORKSHIRE BD21 5EF GB Other 510(k) Applications for this Company
Contact	ANDREW JW WALL Other 510(k) Applications for this Contact
Regulation Number	868.5880   More FDA Info for this Regulation Number
Classification Product Code	CAD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/22/2005
Decision Date	08/23/2005
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	Y
Expedited Review