FDA 510(k) Application Details - K010910

Device Classification Name	Applier, Aneurysm Clip   More FDA Info for this Device
510(K) Number	K010910
Device Name	Applier, Aneurysm Clip
Applicant	MEDICON, E.G. GAENSAECKER 15 TUTTLINGEN D-78532 DE Other 510(k) Applications for this Company
Contact	JOACHIM SCHMID 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	03/26/2001
Decision Date	08/01/2001
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