K252388
- 510(k) number
- K252388
- Device name
- Vanquish Water Vapor Ablation Device
- Applicant
- Francis Medical, Inc. MN · US
- Product code
- KNS — Unit, Electrosurgical, Endoscopic (With Or Without A
- Decision date
- 2025-11-26
- Date received
- 2025-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252388.pdf
Official FDA record: K252388
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.