510(k) K172278 ยท GBM Catheter, Urethral
Firlit-Kluge Urethral Stent, Koyle Diaper Stent, Zaontz Urethral Stent
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Nov 22, 2017 |
| Received | Jul 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172278
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.