K260502
- 510(k) number
- K260502
- Device name
- Liv Pre-lubricated Intermittent Catheter
- Applicant
- HR Healthcare PA · US
- Product code
- EZD — Catheter, Straight
- Decision date
- 2026-03-12
- Date received
- 2026-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260502.pdf
Official FDA record: K260502
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.