K240167
- 510(k) number
- K240167
- Device name
- Single-use Ureteral Access Sheath
- Applicant
- Hunan Vathin Medical Instrument Co., Ltd. CN
- Product code
- FED — Endoscopic Access Overtube, Gastroenterology-Urology
- Decision date
- 2024-10-08
- Date received
- 2024-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K240167.pdf
Official FDA record: K240167
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.