Class Class II

Vanquish Water Vapor Ablation Device (K252388)

K252388 2025-11-26 Traditional
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Description

Vanquish Water Vapor Ablation Device by Francis Medical, Inc., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252388
Clearance Date2025-11-26
Clearance TypeTraditional
Product CodeKNS
Regulation Number876.4300

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