510(k) K180070 ยท GBM Catheter, Urethral
SpeediCath Flex Coude Pro
| Applicant | Coloplast, Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 2, 2018 |
| Received | Jan 9, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180070
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.