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. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K182910.
When did Segmented Esophageal Stent System receive FDA 510(k) clearance?
Segmented Esophageal Stent System received FDA 510(k) clearance on 2019-05-29, under 510(k) number K182910.
Who is the listed applicant for Segmented Esophageal Stent System?
The FDA 510(k) record lists Micro-Tech (Nanjing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Segmented Esophageal Stent System?
The FDA product code for Segmented Esophageal Stent System is ESW.
Other records listing Micro-Tech (Nanjing) Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ESW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.