FDA 510(k) Application Details - K003724

Device Classification Name	Heat-Exchanger, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K003724
Device Name	Heat-Exchanger, Cardiopulmonary Bypass
Applicant	MEDTRONIC VASCULAR 7600 NORTHLAND DR. MINNEAPOLIS, MN 55428 US Other 510(k) Applications for this Company
Contact	MARIE HOLM Other 510(k) Applications for this Contact
Regulation Number	870.4240   More FDA Info for this Regulation Number
Classification Product Code	DTR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/04/2000
Decision Date	12/21/2000
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