FDA 510(k) Application Details - K160403

Device Classification Name	Endoscope Channel Accessory   More FDA Info for this Device
510(K) Number	K160403
Device Name	Endoscope Channel Accessory
Applicant	ENDOCHOICE, INC. 11810 WILLS ROAD ALPHARETTA, GA 30009 US Other 510(k) Applications for this Company
Contact	DANIEL HOEFER Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	ODC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/12/2016
Decision Date	05/19/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review