FDA 510(k) Application Details - K004046

Device Classification Name	Defoamer, Cardiopulmonary Bypass   More FDA Info for this Device
510(K) Number	K004046
Device Name	Defoamer, Cardiopulmonary Bypass
Applicant	COBE CARDIOVASCULAR, INC. 14401 WEST 65TH WAY ARVADA, CO 80004 US Other 510(k) Applications for this Company
Contact	LYNNE LEONARD Other 510(k) Applications for this Contact
Regulation Number	870.4230   More FDA Info for this Regulation Number
Classification Product Code	DTP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/29/2000
Decision Date	04/26/2001
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