FDA 510(k) Application Details - K022880

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K022880
Device Name	Clamp, Vascular
Applicant	GUIDANT CORP. 3744 MT. DIABLO BLVD. SUITE 305 LAFAYETTE, CA 94549 US Other 510(k) Applications for this Company
Contact	JEFF SCHAKENRAAD Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	DXC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/2002
Decision Date	09/13/2002
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	Y
Expedited Review