FDA 510(k) Application Details - K031431

Device Classification Name	Valve, Non-Rebreathing   More FDA Info for this Device
510(K) Number	K031431
Device Name	Valve, Non-Rebreathing
Applicant	BAWMED UK 6 GREAT HOUSE MEADOWS UNITED KINGDOM CF61 ISU. GB Other 510(k) Applications for this Company
Contact	BARBARA WOODS Other 510(k) Applications for this Contact
Regulation Number	868.5870   More FDA Info for this Regulation Number
Classification Product Code	CBP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/06/2003
Decision Date	07/13/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review