K243117
- 510(k) number
- K243117
- Device name
- Digital Video Processor
- Applicant
- Hunan Vathin Medical Instrument Co., Ltd. CN
- Product code
- FGB — Ureteroscope And Accessories, Flexible/Rigid
- Decision date
- 2025-01-29
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
510(k) Summary (official FDA PDF): K243117.pdf
Official FDA record: K243117
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.