FDA 510(k) Application Details - K961836

Device Classification Name	Reservoir, Blood, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K961836
Device Name	Reservoir, Blood, Cardiopulmonary Bypass
Applicant	MEDTRONIC VASCULAR 4633 E. LA PALMA AVE. ANAHEIM, CA 92807 US Other 510(k) Applications for this Company
Contact	DEBRA KRIDNER Other 510(k) Applications for this Contact
Regulation Number	870.4400   More FDA Info for this Regulation Number
Classification Product Code	DTN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/13/1996
Decision Date	11/01/1996
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