FDA 510(k) Application Details - K041076

Device Classification Name	Vaporizer, Anesthesia, Non-Heated   More FDA Info for this Device
510(K) Number	K041076
Device Name	Vaporizer, Anesthesia, Non-Heated
Applicant	PENLON LTD. BARTON LANE ABINGDON OX14 3PH GB Other 510(k) Applications for this Company
Contact	ALAN GREEN 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	04/26/2004
Decision Date	08/09/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review