510(k) K180258 ยท GBM Catheter, Urethral
SpeediCath Standard
| Applicant | Coloplast, Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 25, 2018 |
| Received | Jan 30, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180258
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.