K233591
- 510(k) number
- K233591
- Device name
- Stylus
- Applicant
- Degania Silicone , Ltd. IL
- Product code
- KNT — Tubes, Gastrointestinal (And Accessories)
- Decision date
- 2024-05-31
- Date received
- 2023-11-08
- 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: K233591.pdf
Official FDA record: K233591
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.