FDA 510(k) Application Details - K964017

Device Classification Name	Console, Heart-Lung Machine, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K964017
Device Name	Console, Heart-Lung Machine, Cardiopulmonary Bypass
Applicant	AVECOR CARDIOVASCULAR, INC. 13010 COUNTRY RD. 6 PLYMOUTH, MN 55441 US Other 510(k) Applications for this Company
Contact	DENNIS E STEGER Other 510(k) Applications for this Contact
Regulation Number	870.4220   More FDA Info for this Regulation Number
Classification Product Code	DTQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/07/1996
Decision Date	08/05/1997
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