The following data is part of a premarket notification filed by Ovesco Endoscopy Ag with the FDA for Ftrd System Set.
Device ID | K170867 |
510k Number | K170867 |
Device Name: | FTRD System Set |
Classification | Hemostatic Metal Clip For The Gi Tract |
Applicant | Ovesco Endoscopy AG Dorfackerstrasse 26 Tuebingen, DE 72074 |
Contact | Marc O. Schurr |
Correspondent | Martina Krautwald novineon CRO & Consulting Ltd Dorfackerstrasse 26 Tuebingen, DE 72074 |
Product Code | PKL |
Subsequent Product Code | FDI |
Subsequent Product Code | KNS |
Subsequent Product Code | OCZ |
CFR Regulation Number | 876.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-23 |
Decision Date | 2017-07-25 |