FDA 510(k) Application Details - K013091

Device Classification Name	Motor, Drill, Pneumatic   More FDA Info for this Device
510(K) Number	K013091
Device Name	Motor, Drill, Pneumatic
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	882.4370   More FDA Info for this Regulation Number
Classification Product Code	HBB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/17/2001
Decision Date	01/25/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review