FDA 510(k) Application Details - K112229

Device Classification Name	Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type   More FDA Info for this Device
510(K) Number	K112229
Device Name	Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Applicant	TERUMO CARDIOVASCULAR SYSTEMS 6200 JACKSON RD ANN ARBOR, MI 48103 US Other 510(k) Applications for this Company
Contact	REBECCA ANDERSEN Other 510(k) Applications for this Contact
Regulation Number	870.4360   More FDA Info for this Regulation Number
Classification Product Code	KFM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/03/2011
Decision Date	12/09/2011
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