FDA 510(k) Application Details - K061628

Device Classification Name	Oxygenator, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K061628
Device Name	Oxygenator, Cardiopulmonary Bypass
Applicant	MAQUET CARDIOPULMONARY AG 414 MARYJOE WAY WARRINGTON, PA 18976 US Other 510(k) Applications for this Company
Contact	JAMES COLLIE Other 510(k) Applications for this Contact
Regulation Number	870.4350   More FDA Info for this Regulation Number
Classification Product Code	DTZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/12/2006
Decision Date	08/22/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review