FDA 510(k) Application Details - K170462

Device Classification Name	Endoscope, Neurological   More FDA Info for this Device
510(K) Number	K170462
Device Name	Endoscope, Neurological
Applicant	KARL STORZ Endoscopy-America, Inc. 2151 E. Grand Avenue EI Segundo, CA 90245 US Other 510(k) Applications for this Company
Contact	Susie S. Chen 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	02/15/2017
Decision Date	05/16/2017
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