K241271
- 510(k) number
- K241271
- Device name
- Aqua Medical RF Vapor Ablation System
- Applicant
- Aqua Medical, Inc. CA · US
- Product code
- KNS — Unit, Electrosurgical, Endoscopic (With Or Without A
- Decision date
- 2024-12-12
- Date received
- 2024-05-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241271.pdf
Official FDA record: K241271
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.