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FDA 510(k)

Segmented Esophageal Stent System

K-Number: K182910 · 2019-05-29

Decision Date2019-05-29
Product CodeESW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Segmented Esophageal Stent System is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2019-05-29 under approval number K182910. The device is classified under product code ESW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.