510(k) K192904 ยท GBM Catheter, Urethral
SpeediCath Compact Set
| Applicant | Coloplast, Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 2, 2020 |
| Received | Oct 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192904
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.