FDA 510(k) Application Details - K200770

Device Classification Name	Endoscopic Access Overtube, Gastroenterology-Urology   More FDA Info for this Device
510(K) Number	K200770
Device Name	Endoscopic Access Overtube, Gastroenterology-Urology
Applicant	Trokamed GmbH Kleine Breite 17 Geisingen 78187 DE Other 510(k) Applications for this Company
Contact	Stefan Weiland Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FED Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/25/2020
Decision Date	07/30/2021
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