FDA 510(k) Application Details - K954658

Device Classification Name	Applier, Aneurysm Clip   More FDA Info for this Device
510(K) Number	K954658
Device Name	Applier, Aneurysm Clip
Applicant	VON ZEPPELIN GMBH GISTLSTRASSE 99 PULLACH D-82049 DE Other 510(k) Applications for this Company
Contact	DIETER VON ZEPPELIN Other 510(k) Applications for this Contact
Regulation Number	882.4175   More FDA Info for this Regulation Number
Classification Product Code	HCI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/10/1995
Decision Date	10/08/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review