510(k) K190620 ยท GBM Catheter, Urethral
SpeediCath Flex Coude Pro
| Applicant | Coloplast, Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 10, 2019 |
| Received | Mar 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190620
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.