K251864
- 510(k) number
- K251864
- Device name
- Rubber Utility Catheter
- Applicant
- C.R. Bard, Inc. GA · US
- Product code
- KOD — Catheter, Urological
- Decision date
- 2026-02-23
- Date received
- 2025-06-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251864.pdf
Official FDA record: K251864
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.