FDA 510(k) Application Details - K122844

Device Classification Name	Oxygenator, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K122844
Device Name	Oxygenator, Cardiopulmonary Bypass
Applicant	SORIN GROUP ITALIA S.R.L. 14401 W. 65TH WAY ARVADA, CO 80004 US Other 510(k) Applications for this Company
Contact	SCOTT LIGHT 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	09/17/2012
Decision Date	10/17/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review