FDA 510(k) Application Details - K162330

Device Classification Name	Colonoscope And Accessories, Flexible/Rigid   More FDA Info for this Device
510(K) Number	K162330
Device Name	Colonoscope And Accessories, Flexible/Rigid
Applicant	Medrobotics Corporation 475 Paramount Drive Raynham, MD 02767 US Other 510(k) Applications for this Company
Contact	John D. Bonasera Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FDF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/19/2016
Decision Date	05/04/2017
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