FDA 510(k) Application Details - K961406

Device Classification Name	Endoscope, Neurological   More FDA Info for this Device
510(K) Number	K961406
Device Name	Endoscope, Neurological
Applicant	NEURO NAVIGATIONAL CORP. 3180 PULLMAN ST. COSTA MESA, CA 92626 US Other 510(k) Applications for this Company
Contact	KAREN U SALINAS Other 510(k) Applications for this Contact
Regulation Number	882.1480   More FDA Info for this Regulation Number
Classification Product Code	GWG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/11/1996
Decision Date	06/13/1996
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