FDA 510(k) Application Details - K972689

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K972689
Device Name	Clamp, Vascular
Applicant	ANLAM CORP. 10536-101 ST. EDMONTON, ALBERTA T5H 2R8 CA Other 510(k) Applications for this Company
Contact	ANTHONY LAM 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	07/17/1997
Decision Date	08/27/1998
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