KOD

Catheter, Urological

Product code
KOD
Device name
Catheter, Urological
Device class
Class 2
21 CFR
21 CFR 876.5130
Medical specialty
Gastroenterology, Urology
Marketing pathway
510(K)
Flag
Third-party review eligible
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
238 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2026-02-23.

NumberDecision dateApplicantDevice nameSummary
K2518642026-02-23C.R. Bard, Inc.Rubber Utility CatheterPDF

1 summaries are archived here for direct download.

Official FDA classification page: KOD
Classification and pathway per current FDA publications. Data from openFDA (CC0).