K240853
- 510(k) number
- K240853
- Device name
- Pathfinder® CR System
- Applicant
- Neptune Medical, Inc. CA · US
- Product code
- FED — Endoscopic Access Overtube, Gastroenterology-Urology
- Decision date
- 2024-06-27
- Date received
- 2024-03-28
- Decision
- Unknown
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K240853.pdf
Official FDA record: K240853
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.