K254076
- 510(k) number
- K254076
- Device name
- BD Touchless Plus Unisex Pre-Lubricated Urethral Catheter Kit
- Applicant
- C.R. Bard, Inc. GA · US
- Product code
- FCM — Tray, Catheterization, Sterile Urethral, With Or Wit
- Decision date
- 2026-05-29
- Date received
- 2025-12-18
- Decision
- Unknown
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K254076.pdf
Official FDA record: K254076
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.