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FDA 510(k)

Vanquish Water Vapor Ablation Device

N.º K: K252388 · 2025-11-26

SolicitanteFrancis Medical, Inc.
Fecha de decisión2025-11-26
Código de productoKNS
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Vanquish Water Vapor Ablation Device is the device name listed in this FDA 510(k) record. The listed applicant is Francis Medical, Inc.. It received FDA 510(k) clearance on 2025-11-26 under 510(k) number K252388. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Vanquish Water Vapor Ablation Device?

Vanquish Water Vapor Ablation Device is a medical device that received FDA 510(k) clearance on 2025-11-26. The listed applicant is Francis Medical, Inc.. The 510(k) number is K252388.

When did Vanquish Water Vapor Ablation Device receive FDA 510(k) clearance?

Vanquish Water Vapor Ablation Device received FDA 510(k) clearance on 2025-11-26, under 510(k) number K252388.

Who is the listed applicant for Vanquish Water Vapor Ablation Device?

The FDA 510(k) record lists Francis Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vanquish Water Vapor Ablation Device?

The FDA product code for Vanquish Water Vapor Ablation Device is KNS.

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Fuente oficial

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