K232596
- 510(k) number
- K232596
- Device name
- EndoGI S-Path Biliary Stent System
- Applicant
- Endogi Medical, Ltd. IL
- Product code
- FGE — Stents, Drains And Dilators For The Biliary Ducts
- Decision date
- 2023-09-27
- Date received
- 2023-08-25
- Decision
- Unknown
- Clearance type
- Special
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232596.pdf
Official FDA record: K232596
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.