FDA 510(k) Application Details - K061453

Device Classification Name	Wire, Guide, Catheter   More FDA Info for this Device
510(K) Number	K061453
Device Name	Wire, Guide, Catheter
Applicant	GUIDANT CORP. 4100 Hamline Avenue North St. Paul, MN 55112-5798 US Other 510(k) Applications for this Company
Contact	KATHLEEN VITTUM Other 510(k) Applications for this Contact
Regulation Number	870.1330   More FDA Info for this Regulation Number
Classification Product Code	DQX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/25/2006
Decision Date	06/22/2006
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