FDA 510(k) Application Details - K191029

Device Classification Name	Oxygenator, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K191029
Device Name	Oxygenator, Cardiopulmonary Bypass
Applicant	Medtronic, Inc. 7611 Northland Drive Minneapolis, MN 55428 US Other 510(k) Applications for this Company
Contact	Sammie C Joseph-Fredericks 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	04/18/2019
Decision Date	05/17/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review