FDA 510(k) Application Details - K955827

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K955827
Device Name	Clamp, Vascular
Applicant	Y. DANESHVAR 33433 SIX MILE RD. LIVONIA, MI 48152 US Other 510(k) Applications for this Company
Contact	Y. DANESHVAR 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	12/26/1995
Decision Date	10/02/1996
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