FDA 510(k), K173085, invendoscopy E210 System

510(K) Number: K173085
Device Name: invendoscopy E210 System
Manufacturer: invendo medical GmbH
Device Classification Name: colonoscope and accessories, flexible/rigid
Regulation Number: 876.1500
Classification Product Code: FDF
Date Received: 09/29/2017
Decision Date: 01/08/2018
Regulation Medical Specialty: Gastroenterology/Urology

Total pages: 1171
Fully redacted pages: 1099
Content pages: 72