Segmented Esophageal Stent System
K-Number: K182910 · 2019-05-29
Device Summary
Frequently Asked Questions
What is the Segmented Esophageal Stent System?
Segmented Esophageal Stent System is a medical device that received FDA 510(k) clearance on 2019-05-29. It is manufactured by Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K182910.
When was Segmented Esophageal Stent System approved by the FDA?
Segmented Esophageal Stent System received FDA 510(k) clearance on 2019-05-29, under approval number K182910.
What company makes Segmented Esophageal Stent System?
Segmented Esophageal Stent System is manufactured by Micro-Tech (Nanjing) Co., Ltd..
What is the FDA product code for Segmented Esophageal Stent System?
The FDA product code for Segmented Esophageal Stent System is ESW.
Related Clinical Trials
Other Devices by Micro-Tech (Nanjing) Co., Ltd.
Related Devices (Code: ESW)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.