FDA 510(k) Application Details - K992980

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K992980
Device Name	Clamp, Vascular
Applicant	NOVARE SURGICAL SYSTEMS, INC. 10231 BUBB RD. CUPERTINO, CA 95014 US Other 510(k) Applications for this Company
Contact	NOEL MESSENGER 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	09/03/1999
Decision Date	06/08/2000
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