FDA 510(k) Application Details - K963716

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K963716
Device Name	Clamp, Vascular
Applicant	PERCUTANEOUS TECHNOLOGIES, INC. 773 TROTTER COURT WALNUT, CA 91789 US Other 510(k) Applications for this Company
Contact	WILLIAM MEYER 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	09/16/1996
Decision Date	04/02/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review