FDA 510(k) Application Details - K021958

Device Classification Name	More FDA Info for this Device
510(K) Number	K021958
Device Name	TRELLIS PLUS INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH 20CM (100CM CATHETER LENGTH 10CM INFUSION H
Applicant	BACCHUS VASCULAR, INC. 3110 CORONADO DR. SANTA CLARA, CA 95054 US Other 510(k) Applications for this Company
Contact	GREG MATHINSON Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/14/2002
Decision Date	07/03/2002
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