FDA 510(k) Application Details - K052165

Device Classification Name	Temporary Carotid Catheter For Embolic Capture   More FDA Info for this Device
510(K) Number	K052165
Device Name	Temporary Carotid Catheter For Embolic Capture
Applicant	GUIDANT CORPORATION 3200 Lakeside Drive Santa Clara, CA 95054 US Other 510(k) Applications for this Company
Contact	JULIA ANASTAS Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	NTE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/09/2005
Decision Date	08/16/2005
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