FDA 510(k)

Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System

Número K: K233939 · 2024-04-29

Data da decisão2024-04-29

Código do produtoESW

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific. It received FDA 510(k) clearance on 2024-04-29 under 510(k) number K233939. The device is classified under product code ESW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System?

Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System is a medical device that received FDA 510(k) clearance on 2024-04-29. The listed applicant is Boston Scientific. The 510(k) number is K233939.

When did Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System receive FDA 510(k) clearance?

Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System received FDA 510(k) clearance on 2024-04-29, under 510(k) number K233939.

Who is the listed applicant for Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System?

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

What is the FDA product code for Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System?

The FDA product code for Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System is ESW.

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Dispositivos Relacionados (Código: ESW)

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