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FDA 510(k)

Agile Esophageal Stent System

K-Number: K233837 · 2024-04-04

Decision Date2024-04-04
Product CodeESW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Agile Esophageal Stent System is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2024-04-04 under 510(k) number K233837. 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 Agile Esophageal Stent System?

Agile Esophageal Stent System is a medical device that received FDA 510(k) clearance on 2024-04-04. The listed applicant is Boston Scientific Corporation. The 510(k) number is K233837.

When did Agile Esophageal Stent System receive FDA 510(k) clearance?

Agile Esophageal Stent System received FDA 510(k) clearance on 2024-04-04, under 510(k) number K233837.

Who is the listed applicant for Agile Esophageal Stent System?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Agile Esophageal Stent System?

The FDA product code for Agile Esophageal Stent System is ESW.

Related Clinical Trials

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.

Other records listing Boston Scientific Corporation 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.

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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

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