510(k) K181979 · KOD Catheter, Urological
Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent Catheter
| Applicant | Teleflexmedical, Inc., Morrisville NC, US |
| Decision | Substantially Equivalent, May 24, 2019 |
| Received | Jul 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181979
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.